Variant report

Variant	esv1800060
Chromosome Location	chr1:174132703-174501836
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2572)
CpG islands
(count:428)
Chromatin interactive
region (count:198)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2572 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:174143355-174143434	K562	blood:	n/a	n/a
2	ARID3A	chr1:174186896-174187175	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:174133975-174134175	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:174160161-174160263	K562	blood:	n/a	n/a
5	ARID3A	chr1:174135884-174136567	K562	blood:	n/a	n/a
6	ARID3A	chr1:174243609-174243996	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:174199624-174199775	K562	blood:	n/a	n/a
8	ARID3A	chr1:174227171-174227530	HepG2	liver:	n/a	n/a
9	ARID3A	chr1:174382888-174383024	K562	blood:	n/a	n/a
10	ARID3A	chr1:174174954-174175051	K562	blood:	n/a	n/a
11	ARID3A	chr1:174231871-174232199	HepG2	liver:	n/a	n/a
12	ARID3A	chr1:174231891-174232149	K562	blood:	n/a	n/a
13	ARID3A	chr1:174235526-174236877	HepG2	liver:	n/a	n/a
14	ARID3A	chr1:174396120-174396181	K562	blood:	n/a	n/a
15	ARID3A	chr1:174186888-174187188	K562	blood:	n/a	n/a
16	ARID3A	chr1:174143545-174143778	HepG2	liver:	n/a	n/a
17	ARID3A	chr1:174227162-174227507	K562	blood:	n/a	n/a
18	ARID3A	chr1:174239214-174239484	HepG2	liver:	n/a	n/a
19	ARID3A	chr1:174208511-174209005	HepG2	liver:	n/a	n/a
20	ARID3A	chr1:174174087-174174394	HepG2	liver:	n/a	n/a
21	ATF1	chr1:174397299-174397520	K562	blood:	n/a	n/a
22	ATF1	chr1:174201924-174202155	K562	blood:	n/a	n/a
23	ATF1	chr1:174135815-174136435	K562	blood:	n/a	n/a
24	ATF1	chr1:174199566-174199927	K562	blood:	n/a	n/a
25	ATF1	chr1:174428850-174428929	K562	blood:	n/a	n/a
26	ATF1	chr1:174277912-174277913	K562	blood:	n/a	n/a
27	ATF1	chr1:174448222-174448255	K562	blood:	n/a	n/a
28	ATF1	chr1:174173860-174174306	K562	blood:	n/a	n/a
29	ATF1	chr1:174235618-174235768	K562	blood:	n/a	n/a
30	ATF1	chr1:174263197-174263318	K562	blood:	n/a	n/a
31	ATF1	chr1:174169246-174169307	K562	blood:	n/a	n/a
32	ATF1	chr1:174493199-174493227	K562	blood:	n/a	n/a
33	ATF1	chr1:174484804-174484808	K562	blood:	n/a	n/a
34	ATF2	chr1:174367318-174367778	GM12878	blood:	n/a	n/a
35	ATF2	chr1:174135889-174137189	GM12878	blood:	n/a	n/a
36	ATF2	chr1:174178688-174179318	GM12878	blood:	n/a	n/a
37	ATF2	chr1:174245148-174245601	GM12878	blood:	n/a	n/a
38	ATF2	chr1:174175487-174176060	GM12878	blood:	n/a	n/a
39	ATF2	chr1:174173746-174174313	GM12878	blood:	n/a	n/a
40	ATF2	chr1:174367341-174367790	GM12878	blood:	n/a	n/a
41	ATF2	chr1:174143787-174144215	GM12878	blood:	n/a	n/a
42	ATF2	chr1:174173585-174174478	GM12878	blood:	n/a	n/a
43	ATF2	chr1:174135981-174137121	GM12878	blood:	n/a	n/a
44	BACH1	chr1:174181908-174182084	K562	blood:	n/a	n/a
45	BACH1	chr1:174186513-174186786	K562	blood:	n/a	n/a
46	BACH1	chr1:174180646-174180687	K562	blood:	n/a	n/a
47	BACH1	chr1:174414983-174415353	H1-hESC	embryonic stem cell:	n/a	n/a
48	BACH1	chr1:174174011-174174379	K562	blood:	n/a	n/a
49	BACH1	chr1:174159638-174159721	K562	blood:	n/a	n/a
50	BACH1	chr1:174192832-174192848	K562	blood:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:174319673-174319723	NB4	blood:	n/a
2	chr1:174319673-174319723	NB4	blood:	n/a
3	chr1:174417175-174417225	MCF-7	breast:	n/a
4	chr1:174319673-174319723	SAEC	small airway:	n/a
5	chr1:174186816-174186866	HRCEpiC	kidney:	n/a
6	chr1:174417967-174418017	MCF10A-Er-Src	breast:	n/a
7	chr1:174417375-174417425	HNPCEpiC	eye:	n/a
8	chr1:174319673-174319723	GM12878	blood:	n/a
9	chr1:174319673-174319723	AG09309	skin:	n/a
10	chr1:174417375-174417425	RPTEC	kidney:	n/a
11	chr1:174417175-174417225	HCF	heart:	n/a
12	chr1:174208162-174208212	HMEC	breast:	n/a
13	chr1:174319673-174319723	RPTEC	kidney:	n/a
14	chr1:174352684-174352734	NHBE	bronchial:	n/a
15	chr1:174417967-174418017	HMEC	breast:	n/a
16	chr1:174417375-174417425	PFSK-1	brain:	n/a
17	chr1:174208162-174208212	H1-hESC	embryonic stem cell:	embryo
18	chr1:174208162-174208212	PANC-1	pancreas:	n/a
19	chr1:174208162-174208212	CMK	blood:	n/a
20	chr1:174186816-174186866	HEK293	kidney:	embryo
21	chr1:174208162-174208212	IMR90	lung:	fetal
22	chr1:174319673-174319723	AG10803	skin:	n/a
23	chr1:174417375-174417425	MCF10A-Er-Src	breast:	n/a
24	chr1:174186816-174186866	HPAEpiC	pulmonary alveolar:	n/a
25	chr1:174352684-174352734	LNCaP	prostate:	n/a
26	chr1:174208162-174208212	HAEpiC	amniotic membrane:	n/a
27	chr1:174352684-174352734	HCF	heart:	n/a
28	chr1:174352684-174352734	Jurkat	blood:	n/a
29	chr1:174417967-174418017	HIPEpiC	eye:	n/a
30	chr1:174417175-174417225	A549	lung:	n/a
31	chr1:174208162-174208212	HPAEpiC	pulmonary alveolar:	n/a
32	chr1:174417967-174418017	Caco-2	colon:	n/a
33	chr1:174186816-174186866	AG04450	lung:	fetal
34	chr1:174352684-174352734	HIPEpiC	eye:	n/a
35	chr1:174417175-174417225	Caco-2	colon:	n/a
36	chr1:174186816-174186866	PrEC	prostate:	n/a
37	chr1:174208162-174208212	HRPEpiC	eye:	n/a
38	chr1:174352684-174352734	HCPEpiC	choroid plexus:	n/a
39	chr1:174417375-174417425	HIPEpiC	eye:	n/a
40	chr1:174186816-174186866	PFSK-1	brain:	n/a
41	chr1:174417967-174418017	HEK293	kidney:	embryo
42	chr1:174352684-174352734	Caco-2	colon:	n/a
43	chr1:174208162-174208212	SK-N-SH	brain:	n/a
44	chr1:174352684-174352734	SK-N-SH	brain:	n/a
45	chr1:174352684-174352734	HRPEpiC	eye:	n/a
46	chr1:174352684-174352734	NT2-D1	testis:	n/a
47	chr1:174417967-174418017	HNPCEpiC	eye:	n/a
48	chr1:174417967-174418017	NB4	blood:	n/a
49	chr1:174208162-174208212	BJ	skin:	n/a
50	chr1:174417967-174418017	GM06990	blood:	n/a

(count:198 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr1:174185151..174188008-chr1:174194442..174198142,3	K562	blood:
2	chr1:174420628..174423006-chr1:174424339..174426436,2	K562	blood:
3	chr1:174382438..174383401-chr1:174695381..174696315,3	MCF-7	breast:
4	chr1:174209681..174211217-chr1:174211648..174214510,2	K562	blood:
5	chr1:174412862..174415441-chr1:174418910..174422017,3	K562	blood:
6	chr1:174132073..174134827-chr1:174138516..174140914,3	MCF-7	breast:
7	chr1:174132422..174134111-chr1:174800626..174802567,2	K562	blood:
8	chr1:174225306..174226872-chr1:174233081..174234854,2	K562	blood:
9	chr1:174485495..174487649-chr1:174503565..174506456,2	K562	blood:
10	chr1:174382494..174383374-chr1:174713222..174713791,2	MCF-7	breast:
11	chr1:174186060..174188372-chr1:174193893..174195942,2	K562	blood:
12	chr1:174412862..174415441-chr1:174418910..174422017,3	K562	blood:
13	chr1:174293187..174295185-chr1:174300416..174302383,2	K562	blood:
14	chr1:174231956..174232498-chr1:174695300..174696266,2	MCF-7	breast:
15	chr1:174128707..174130217-chr1:174164709..174166414,2	K562	blood:
16	chr1:174287001..174289924-chr1:174290747..174293393,2	K562	blood:
17	chr1:174136409..174138753-chr1:174139089..174145165,6	K562	blood:
18	chr1:174149924..174151472-chr1:174154345..174156878,2	K562	blood:
19	chr1:174193716..174196579-chr1:174196717..174200011,3	MCF-7	breast:
20	chr1:174501105..174504016-chr1:174516125..174518683,2	K562	blood:
21	chr1:174158960..174161694-chr1:174164662..174167169,2	K562	blood:
22	chr1:174208598..174210493-chr1:174218021..174220094,2	MCF-7	breast:
23	chr1:174420516..174421195-chr1:174712811..174713329,2	MCF-7	breast:
24	chr1:173835071..173837781-chr1:174150428..174152457,2	K562	blood:
25	chr1:174478227..174480621-chr1:174484949..174486891,2	MCF-7	breast:
26	chr1:174361556..174363386-chr1:174366777..174369174,2	K562	blood:
27	chr1:174468172..174471596-chr1:174473522..174476530,3	K562	blood:
28	chr1:174226899..174227872-chr1:174716763..174717382,2	MCF-7	breast:
29	chr1:174127794..174129583-chr1:174152496..174155394,2	K562	blood:
30	chr1:174126773..174130158-chr1:174148620..174150674,4	K562	blood:
31	chr1:173951962..173954663-chr1:174137469..174140285,2	K562	blood:
32	chr1:174152071..174154187-chr1:174154617..174157580,2	K562	blood:
33	chr1:174320271..174322217-chr1:174328823..174331200,2	MCF-7	breast:
34	chr1:174320271..174322217-chr1:174328823..174331200,2	MCF-7	breast:
35	chr1:174128029..174130536-chr1:174135195..174136923,2	MCF-7	breast:
36	chr1:174152071..174154187-chr1:174154617..174157580,2	K562	blood:
37	chr1:174128679..174131569-chr1:174177362..174180012,2	K562	blood:
38	chr1:174227280..174227817-chr1:174712805..174713329,2	K562	blood:
39	chr1:174403554..174404054-chr10:47655569..47656367,2	NB4	blood:
40	chr1:174148713..174151052-chr1:174207157..174208937,2	MCF-7	breast:
41	chr1:174122708..174125565-chr1:174154961..174157187,2	K562	blood:
42	chr1:174225306..174226872-chr1:174233081..174234854,2	K562	blood:
43	chr1:174127362..174130761-chr1:174131482..174135069,5	MCF-7	breast:
44	chr1:173792385..173795057-chr1:174174691..174177146,2	K562	blood:
45	chr1:173990518..173992302-chr1:174184021..174186918,2	MCF-7	breast:
46	chr1:174215485..174217028-chr1:174218870..174220698,2	MCF-7	breast:
47	chr1:174181164..174182677-chr1:174184140..174185798,2	K562	blood:
48	chr1:174193716..174196579-chr1:174196717..174200011,3	MCF-7	breast:
49	chr1:174156183..174157757-chr1:174183127..174185978,2	K562	blood:
50	chr1:174188636..174191430-chr1:174968395..174970624,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RC3H1-4	chr1:174336243-174337177	NONHSAT007733
2	lnc-RC3H1-3	chr1:174144306-174144529	NONHSAT007727
3	lnc-RC3H1-3	chr1:174156215-174156272	NONHSAT007727
4	lnc-RC3H1-3	chr1:174140521-174140895	NONHSAT007727

No data

Variant related genes	Relation type
ENSG00000237317	TF binding region
GPR52	TF binding region
ENSG00000227373	TF binding region
RABGAP1L	TF binding region
ENSG00000266125	TF binding region
ENSG00000238872	TF binding region
ENSG00000237317	CpG island
GPR52	CpG island
ENSG00000227373	CpG island
RABGAP1L	CpG island
ENSG00000266125	CpG island
ENSG00000238872	CpG island
ENSG00000227373	chromatin interactions
ENSG00000120334	chromatin interactions
ENSG00000117593	chromatin interactions
ENSG00000116161	chromatin interactions
ENSG00000185278	chromatin interactions
ENSG00000208317	chromatin interactions
ENSG00000224977	chromatin interactions
ENSG00000259942	chromatin interactions
ENSG00000234741	chromatin interactions
ENSG00000203737	chromatin interactions
ENSG00000152061	chromatin interactions
ENSG00000135870	chromatin interactions

Extended variants
information (count: 12763 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:12763 , 50 per page) page: 1 2 3 4 5 6 7 ... 256

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13375674	chr1:174132703-174132704	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs531913771	chr1:174132744-174132745	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs58431458	chr1:174132750-174132751	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs36027110	chr1:174132763-174132764	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs548521829	chr1:174132838-174132839	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs554540049	chr1:174132906-174132907	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs76547958	chr1:174132916-174132917	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs34159764	chr1:174132934-174132935	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs557235189	chr1:174132948-174132949	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs35853168	chr1:174132975-174132976	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs61288130	chr1:174133008-174133009	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs187332027	chr1:174133035-174133036	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs376259298	chr1:174133041-174133042	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs553693201	chr1:174133069-174133070	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs373974675	chr1:174133077-174133078	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs572898783	chr1:174133091-174133092	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs191331568	chr1:174133101-174133102	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs554725368	chr1:174133162-174133163	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs184480870	chr1:174133166-174133167	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs565955465	chr1:174133236-174133237	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs13375690	chr1:174133251-174133252	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs138547177	chr1:174133294-174133295	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs61827904	chr1:174133327-174133328	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs559203820	chr1:174133340-174133341	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs528492642	chr1:174133395-174133396	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs189549715	chr1:174133454-174133455	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs568551937	chr1:174133471-174133472	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs530864307	chr1:174133504-174133505	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs373620927	chr1:174133510-174133511	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs551052831	chr1:174133583-174133584	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs575190778	chr1:174133589-174133590	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs148742333	chr1:174133591-174133592	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs149265728	chr1:174133685-174133686	Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs79182618	chr1:174133697-174133698	Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs147979354	chr1:174133738-174133739	Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs567143846	chr1:174133764-174133765	Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs536165739	chr1:174133781-174133782	Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs554563300	chr1:174133816-174133817	Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs181933097	chr1:174133830-174133831	Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs368544268	chr1:174133834-174133835	Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs536792360	chr1:174133847-174133848	Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs557006406	chr1:174133864-174133865	Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs78001752	chr1:174133959-174133960	Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs554903687	chr1:174133970-174133971	Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs372607712	chr1:174134151-174134152	Weak transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs572762908	chr1:174134260-174134261	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs185733993	chr1:174134269-174134270	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs541826662	chr1:174134360-174134361	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs539693339	chr1:174134367-174134368	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs561989806	chr1:174134409-174134410	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20838587	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	19404257	CNVD

Chromatin state (count:3169 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:174129600-174134000	Weak transcription	Stomach Mucosa	stomach
2	chr1:174129600-174164800	Weak transcription	Gastric	stomach
3	chr1:174129600-174173200	Weak transcription	Pancreas	Pancrea
4	chr1:174129800-174133200	Weak transcription	Small Intestine	intestine
5	chr1:174129800-174134800	Weak transcription	Ovary	ovary
6	chr1:174129800-174135000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr1:174129800-174135000	Weak transcription	Stomach Smooth Muscle	stomach
8	chr1:174129800-174135000	Weak transcription	Spleen	Spleen
9	chr1:174129800-174137000	Weak transcription	Fetal Lung	lung
10	chr1:174129800-174145600	Weak transcription	Fetal Thymus	thymus
11	chr1:174129800-174147000	Weak transcription	Fetal Brain Male	brain
12	chr1:174129800-174149600	Weak transcription	Aorta	Aorta
13	chr1:174130000-174133200	Weak transcription	Colonic Mucosa	Colon
14	chr1:174130000-174133200	Weak transcription	Fetal Intestine Large	intestine
15	chr1:174130000-174133200	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr1:174130000-174133600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr1:174130000-174134800	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr1:174130000-174134800	Weak transcription	Adipose Nuclei	Adipose
19	chr1:174130000-174134800	Weak transcription	Liver	Liver
20	chr1:174130000-174134800	Weak transcription	Brain Hippocampus Middle	brain
21	chr1:174130000-174135400	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr1:174130000-174135400	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr1:174130000-174135800	Weak transcription	Right Ventricle	heart
24	chr1:174130000-174136200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr1:174130000-174144400	Weak transcription	Primary hematopoietic stem cells	blood
26	chr1:174130000-174157600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr1:174130200-174133000	Weak transcription	Fetal Intestine Small	intestine
28	chr1:174130200-174133200	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr1:174130200-174133200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr1:174130200-174133400	Weak transcription	A549	lung
31	chr1:174130200-174135200	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr1:174130200-174135400	Weak transcription	Monocytes-CD14+_RO01746	blood
33	chr1:174130200-174138000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr1:174130200-174143200	Weak transcription	Primary B cells from cord blood	blood
35	chr1:174130200-174145000	Weak transcription	NHEK	skin
36	chr1:174130200-174145600	Weak transcription	Fetal Stomach	stomach
37	chr1:174130200-174147400	Weak transcription	Hela-S3	cervix
38	chr1:174130800-174134800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr1:174130800-174138200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr1:174130800-174156600	Weak transcription	Primary T cells from cord blood	blood
41	chr1:174131000-174135400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr1:174131200-174133200	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr1:174131200-174134600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr1:174131200-174135000	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr1:174131200-174138800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr1:174131400-174136600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr1:174131800-174133000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr1:174131800-174133000	Weak transcription	Duodenum Mucosa	Duodenum
49	chr1:174131800-174133000	Weak transcription	Fetal Heart	heart
50	chr1:174131800-174133200	Weak transcription	HepG2	liver

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