Variant report

Variant	esv1797294
Chromosome Location	chr7:38377067-38406167
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1592)
CpG islands
(count:488)
Chromatin interactive
region (count:15)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1592 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:38380924-38381236	K562	blood:	n/a	n/a
2	ATF1	chr7:38389490-38389669	K562	blood:	n/a	n/a
3	ATF1	chr7:38379898-38380061	K562	blood:	n/a	n/a
4	ATF1	chr7:38380742-38381291	K562	blood:	n/a	n/a
5	BATF	chr7:38389336-38389771	GM12878	blood:	n/a	n/a
6	BATF	chr7:38397831-38398310	GM12878	blood:	n/a	n/a
7	BATF	chr7:38385112-38385446	GM12878	blood:	n/a	n/a
8	BATF	chr7:38393728-38393936	GM12878	blood:	n/a	n/a
9	BATF	chr7:38397936-38398227	GM12878	blood:	n/a	n/a
10	BATF	chr7:38402249-38402527	GM12878	blood:	n/a	chr7:38402448-38402459
11	BATF	chr7:38393104-38393355	GM12878	blood:	n/a	n/a
12	BATF	chr7:38388801-38389033	GM12878	blood:	n/a	n/a
13	BATF	chr7:38384447-38384746	GM12878	blood:	n/a	n/a
14	BATF	chr7:38388739-38389137	GM12878	blood:	n/a	n/a
15	BATF	chr7:38384403-38384723	GM12878	blood:	n/a	n/a
16	BATF	chr7:38393104-38393312	GM12878	blood:	n/a	n/a
17	BATF	chr7:38402244-38402635	GM12878	blood:	n/a	chr7:38402448-38402459
18	BATF	chr7:38398491-38398925	GM12878	blood:	n/a	n/a
19	BCL11A	chr7:38402227-38402452	GM12878	blood:	n/a	chr7:38402374-38402383
20	BCL11A	chr7:38398493-38398682	GM12878	blood:	n/a	n/a
21	BCL11A	chr7:38384321-38384734	GM12878	blood:	n/a	chr7:38384540-38384549
22	BCL11A	chr7:38393701-38393947	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:38397653-38398122	GM12878	blood:	n/a	chr7:38398022-38398031
24	BCLAF1	chr7:38385200-38385540	GM12878	blood:	n/a	n/a
25	BCLAF1	chr7:38389556-38389732	GM12878	blood:	n/a	n/a
26	BHLHE40	chr7:38389643-38389696	GM12878	blood:	n/a	n/a
27	BHLHE40	chr7:38403131-38403176	GM12878	blood:	n/a	n/a
28	BHLHE40	chr7:38380767-38381281	K562	blood:	n/a	n/a
29	BHLHE40	chr7:38379902-38380060	K562	blood:	n/a	n/a
30	BHLHE40	chr7:38403094-38403268	K562	blood:	n/a	n/a
31	BHLHE40	chr7:38393917-38394132	K562	blood:	n/a	n/a
32	BHLHE40	chr7:38398804-38399002	K562	blood:	n/a	n/a
33	BHLHE40	chr7:38385332-38385486	K562	blood:	n/a	n/a
34	BHLHE40	chr7:38385297-38385497	GM12878	blood:	n/a	n/a
35	CBX3	chr7:38398578-38399039	K562	blood:	n/a	n/a
36	CBX3	chr7:38380820-38381270	K562	blood:	n/a	n/a
37	CBX3	chr7:38389461-38389863	K562	blood:	n/a	n/a
38	CBX3	chr7:38403002-38403403	K562	blood:	n/a	n/a
39	CBX3	chr7:38380733-38381387	K562	blood:	n/a	n/a
40	CBX3	chr7:38393853-38394294	K562	blood:	n/a	n/a
41	CCNT2	chr7:38380858-38381223	K562	blood:	n/a	n/a
42	CEBPB	chr7:38402455-38402609	HepG2	liver:	n/a	n/a
43	CEBPB	chr7:38400447-38400672	A549	lung:	n/a	n/a
44	CEBPB	chr7:38380943-38381315	K562	blood:	n/a	n/a
45	CEBPB	chr7:38391385-38391451	IMR90	lung:	n/a	n/a
46	CEBPD	chr7:38380772-38381308	K562	blood:	n/a	n/a
47	CHD1	chr7:38389454-38389506	GM12878	blood:	n/a	n/a
48	CHD1	chr7:38402581-38402583	GM12878	blood:	n/a	n/a
49	CHD2	chr7:38385235-38385424	GM12878	blood:	n/a	n/a
50	CHD2	chr7:38381821-38382011	K562	blood:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38398839-38398889	HRPEpiC	eye:	n/a
2	chr7:38380582-38380632	HNPCEpiC	eye:	n/a
3	chr7:38403507-38403557	ECC-1	luminal epithelium:	n/a
4	chr7:38398836-38398886	ECC-1	luminal epithelium:	n/a
5	chr7:38380582-38380632	GM12891	blood:	n/a
6	chr7:38403507-38403557	NH-A	brain:	n/a
7	chr7:38398839-38398889	SAEC	small airway:	n/a
8	chr7:38389659-38389709	NHDF-neo	bronchial:	n/a
9	chr7:38380582-38380632	CMK	blood:	n/a
10	chr7:38398836-38398886	GM12892	blood:	n/a
11	chr7:38398839-38398889	HIPEpiC	eye:	n/a
12	chr7:38380487-38380537	AG04450	lung:	fetal
13	chr7:38389659-38389709	HCM	heart:	n/a
14	chr7:38380582-38380632	PFSK-1	brain:	n/a
15	chr7:38398836-38398886	SAEC	small airway:	n/a
16	chr7:38389685-38389735	A549	lung:	n/a
17	chr7:38403507-38403557	PrEC	prostate:	n/a
18	chr7:38380487-38380537	AG04449	skin:	fetal
19	chr7:38398836-38398886	LNCaP	prostate:	n/a
20	chr7:38403507-38403557	H1-hESC	embryonic stem cell:	embryo
21	chr7:38398839-38398889	HL-60	blood:	n/a
22	chr7:38380582-38380632	HRPEpiC	eye:	n/a
23	chr7:38380487-38380537	HNPCEpiC	eye:	n/a
24	chr7:38389685-38389735	T-47D	breast:	n/a
25	chr7:38403507-38403557	GM06990	blood:	n/a
26	chr7:38380582-38380632	HUVEC	blood vessel:	n/a
27	chr7:38389659-38389709	GM12891	blood:	n/a
28	chr7:38380487-38380537	Jurkat	blood:	n/a
29	chr7:38398836-38398886	HRPEpiC	eye:	n/a
30	chr7:38389659-38389709	AG10803	skin:	n/a
31	chr7:38389991-38390041	ProgFib	skin:	n/a
32	chr7:38398836-38398886	BJ	skin:	n/a
33	chr7:38403507-38403557	IMR90	lung:	fetal
34	chr7:38403507-38403557	HCF	heart:	n/a
35	chr7:38380582-38380632	T-47D	breast:	n/a
36	chr7:38380582-38380632	A549	lung:	n/a
37	chr7:38380582-38380632	SK-N-SH_RA	brain:	n/a
38	chr7:38403507-38403557	BE2_C	brain:	n/a
39	chr7:38389659-38389709	NB4	blood:	n/a
40	chr7:38389685-38389735	HCM	heart:	n/a
41	chr7:38398836-38398886	MCF10A-Er-Src	breast:	n/a
42	chr7:38398839-38398889	HMEC	breast:	n/a
43	chr7:38380582-38380632	NT2-D1	testis:	n/a
44	chr7:38389685-38389735	IMR90	lung:	fetal
45	chr7:38398836-38398886	PANC-1	pancreas:	n/a
46	chr7:38389685-38389735	PFSK-1	brain:	n/a
47	chr7:38380487-38380537	SK-N-SH	brain:	n/a
48	chr7:38389991-38390041	HL-60	blood:	n/a
49	chr7:38380487-38380537	U87	brain:	n/a
50	chr7:38389991-38390041	ECC-1	luminal epithelium:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:
2	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:
3	chr7:38385094..38385817-chr7:38407469..38408173,2	MCF-7	breast:
4	chr7:38375070..38375771-chr7:38393808..38394547,2	MCF-7	breast:
5	chr7:38369534..38372460-chr7:38378778..38381886,3	K562	blood:
6	chr7:38379860..38381671-chr7:38382000..38383618,2	K562	blood:
7	chr7:38378347..38380949-chr7:38392502..38394879,2	K562	blood:
8	chr7:38269978..38272526-chr7:38377435..38379545,2	K562	blood:
9	chr7:38146965..38147587-chr7:38385316..38385987,2	MCF-7	breast:
10	chr7:38268103..38269784-chr7:38382757..38385051,2	K562	blood:
11	chr7:38378347..38380949-chr7:38392502..38394879,2	K562	blood:
12	chr7:38380741..38382401-chr7:38383649..38386131,2	K562	blood:
13	chr7:38372590..38377698-chr7:38377994..38383669,12	K562	blood:
14	chr7:38378957..38381571-chr7:38387227..38389473,2	K562	blood:
15	chr7:38372590..38377698-chr7:38377994..38383669,12	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STARD3NL-3	chr7:38397521-38397735	NONHSAT120182
2	lnc-STARD3NL-4	chr7:38400418-38400732	NONHSAT120183
3	lnc-STARD3NL-1	chr7:38389947-38390051	ENSG00000250924
4	lnc-STARD3NL-1	chr7:38385622-38385728	ENSG00000250924
5	lnc-STARD3NL-6	chr7:38405093-38405440	NONHSAT120185
6	lnc-STARD3NL-7	chr7:38405699-38406016	NONHSAT120186
7	lnc-STARD3NL-1	chr7:38381683-38384763	ucscGeneNc_uc003tgp_1
8	lnc-AMPH-3	chr7:38395172-38395463	NONHSAT120181
9	lnc-STARD3NL-1	chr7:38381098-38381400	NONHSAT120178
10	lnc-STARD3NL-1	chr7:38381747-38382154	NONHSAT120178
11	lnc-STARD3NL-1	chr7:38381216-38381400	ENSG00000250924
12	lnc-STARD3NL-1	chr7:38389947-38390051	NONHSAT120179
13	lnc-STARD3NL-5	chr7:38404346-38404812	NONHSAT120184
14	lnc-STARD3NL-1	chr7:38381178-38381400	NONHSAT120179
15	lnc-AMPH-4	chr7:38394799-38395026	NONHSAT120180
16	lnc-STARD3NL-1	chr7:38385622-38385728	NONHSAT120179

No data

Variant related genes	Relation type
TRGV2	TF binding region
TRGV7	TF binding region
TRGV5	TF binding region
TRGV6	TF binding region
TRGV4	TF binding region
TRGV3	TF binding region
TRGV5P	TF binding region
TRGV2	CpG island
TRGV7	CpG island
TRGV5	CpG island
TRGV6	CpG island
TRGV4	CpG island
TRGV3	CpG island
TRGV5P	CpG island
ENSG00000211696	chromatin interactions
ENSG00000226212	chromatin interactions
ENSG00000211701	chromatin interactions
ENSG00000228668	chromatin interactions
ENSG00000211697	chromatin interactions
ENSG00000211698	chromatin interactions
ENSG00000249978	chromatin interactions
CA13	miRNA target sites
RAB5A	miRNA target sites
SERTAD3	miRNA target sites

Extended variants
information (count: 1884 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1884 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571202179	chr7:38377081-38377082	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs73694029	chr7:38377090-38377091	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs10228749	chr7:38377125-38377126	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs550733214	chr7:38377142-38377143	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs184939984	chr7:38377146-38377147	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs576954480	chr7:38377173-38377174	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs536467453	chr7:38377190-38377191	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs151009942	chr7:38377215-38377216	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs566187405	chr7:38377253-38377254	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs541110717	chr7:38377260-38377261	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs556944440	chr7:38377322-38377323	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs189613187	chr7:38377402-38377403	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs558231469	chr7:38377434-38377435	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs181880879	chr7:38377535-38377536	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs115601921	chr7:38377542-38377543	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs527936016	chr7:38377575-38377576	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs553130498	chr7:38377657-38377658	Weak transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs77481287	chr7:38377709-38377710	Weak transcription Enhancers Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs369427893	chr7:38377710-38377711	Weak transcription Enhancers Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs75618451	chr7:38377729-38377730	Weak transcription Enhancers Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs397947511	chr7:38377731-38377732	Weak transcription Enhancers Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs574126223	chr7:38377768-38377769	Weak transcription Enhancers Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs186899283	chr7:38377782-38377783	Weak transcription Enhancers Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs376258362	chr7:38377800-38377801	Weak transcription Enhancers Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs572646235	chr7:38377814-38377815	Weak transcription Enhancers Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs189791608	chr7:38377828-38377829	Weak transcription Enhancers Genic enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs2735152	chr7:38377839-38377840	Weak transcription Enhancers Genic enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs56023730	chr7:38377854-38377855	Weak transcription Enhancers Genic enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs147828775	chr7:38377874-38377875	Weak transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs561237538	chr7:38377881-38377882	Weak transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs529809638	chr7:38377907-38377908	Weak transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs370343600	chr7:38377914-38377915	Weak transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs111393946	chr7:38377915-38377916	Weak transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs181336943	chr7:38377924-38377925	Weak transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs4723745	chr7:38377925-38377926	Weak transcription Enhancers Genic enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs184973533	chr7:38378008-38378009	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs571517763	chr7:38378009-38378010	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs537476005	chr7:38378042-38378043	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs557325842	chr7:38378047-38378048	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs112583256	chr7:38378056-38378057	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs146504440	chr7:38378142-38378143	Weak transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs76116215	chr7:38378217-38378218	Weak transcription Enhancers Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs554898498	chr7:38378224-38378225	Weak transcription Enhancers Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs145777447	chr7:38378240-38378241	Weak transcription Enhancers Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs189728618	chr7:38378245-38378246	Weak transcription Enhancers Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs546131819	chr7:38378252-38378253	Weak transcription Enhancers Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs183095373	chr7:38378268-38378269	Weak transcription Enhancers Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs565011525	chr7:38378270-38378271	Weak transcription Enhancers Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs73115859	chr7:38378303-38378304	Weak transcription Enhancers Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs2735151	chr7:38378305-38378306	Weak transcription Enhancers Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Sezary syndrome	18413736	CNVD
Gastric cancer	24379144	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:789 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38371800-38380600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr7:38374200-38377600	Enhancers	Placenta	Placenta
3	chr7:38375400-38377600	Flanking Active TSS	K562	blood
4	chr7:38375400-38380800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr7:38375600-38377400	Enhancers	Fetal Thymus	thymus
6	chr7:38375600-38380000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr7:38375600-38380000	Weak transcription	Spleen	Spleen
8	chr7:38375800-38377400	Enhancers	Primary hematopoietic stem cells	blood
9	chr7:38375800-38377400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
10	chr7:38375800-38378200	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr7:38375800-38379800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr7:38375800-38380000	Weak transcription	Fetal Muscle Trunk	muscle
13	chr7:38375800-38380400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr7:38375800-38380400	Weak transcription	A549	lung
15	chr7:38375800-38380800	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr7:38375800-38380800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr7:38375800-38380800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr7:38375800-38380800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr7:38376000-38377400	Enhancers	Dnd41	blood
20	chr7:38376000-38378200	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr7:38376000-38379800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr7:38376000-38379800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr7:38376000-38380000	Weak transcription	Fetal Stomach	stomach
24	chr7:38376000-38380400	Weak transcription	Fetal Muscle Leg	muscle
25	chr7:38376000-38380400	Weak transcription	Thymus	Thymus
26	chr7:38376000-38380400	Weak transcription	GM12878-XiMat	blood
27	chr7:38376000-38380600	Weak transcription	Adipose Nuclei	Adipose
28	chr7:38376200-38378200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
29	chr7:38376200-38379800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr7:38376400-38379800	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr7:38376400-38379800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
32	chr7:38376400-38380600	Weak transcription	Primary B cells from cord blood	blood
33	chr7:38376400-38381000	Weak transcription	Duodenum Mucosa	Duodenum
34	chr7:38376600-38377400	Enhancers	Primary T cells fromperipheralblood	blood
35	chr7:38376600-38377400	Enhancers	Fetal Intestine Small	intestine
36	chr7:38376600-38377400	Weak transcription	Small Intestine	intestine
37	chr7:38376600-38377600	Enhancers	Fetal Intestine Large	intestine
38	chr7:38376600-38378200	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr7:38376600-38379800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr7:38376600-38380000	Weak transcription	Primary T helper cells fromperipheralblood	blood
41	chr7:38376600-38380600	Weak transcription	Primary B cells from peripheral blood	blood
42	chr7:38376800-38377200	Weak transcription	Pancreas	Pancrea
43	chr7:38376800-38378200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr7:38376800-38379800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr7:38376800-38380800	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr7:38377000-38377600	Active TSS	Primary T killer memory cells from peripheral blood	blood
47	chr7:38377000-38377800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr7:38377000-38379600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr7:38377000-38379800	Weak transcription	Primary T cells from cord blood	blood
50	chr7:38377200-38377400	Enhancers	Brain Hippocampus Middle	brain

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