Variant report

Variant	esv3376035
Chromosome Location	chr10:49673571-49676119
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:52)
CpG islands
(count:366)
Chromatin interactive
region (count:3)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:52 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:49675990-49676555	K562	blood:	n/a	n/a
2	ATF1	chr10:49676060-49676637	K562	blood:	n/a	n/a
3	CBX3	chr10:49676033-49676786	K562	blood:	n/a	n/a
4	CEBPD	chr10:49676046-49676758	K562	blood:	n/a	n/a
5	CEBPD	chr10:49676062-49676698	K562	blood:	n/a	n/a
6	CUX1	chr10:49676073-49676622	K562	blood:	n/a	n/a
7	E2F6	chr10:49674615-49675127	H1-hESC	embryonic stem cell:	n/a	chr10:49674740-49674750
8	E2F6	chr10:49674615-49675207	H1-hESC	embryonic stem cell:	n/a	chr10:49674740-49674750
9	EP300	chr10:49675961-49676872	K562	blood:	n/a	n/a
10	GATA2	chr10:49676106-49676691	K562	blood:	n/a	n/a
11	HMGN3	chr10:49674283-49674479	K562	blood:	n/a	n/a
12	IRF1	chr10:49675974-49676778	K562	blood:	n/a	n/a
13	MAFF	chr10:49675704-49676741	K562	blood:	n/a	n/a
14	MAFK	chr10:49675723-49676608	K562	blood:	n/a	n/a
15	MAX	chr10:49676109-49676657	K562	blood:	n/a	n/a
16	MAX	chr10:49676089-49676691	K562	blood:	n/a	n/a
17	MAX	chr10:49674596-49675191	H1-hESC	embryonic stem cell:	n/a	n/a
18	MAX	chr10:49676069-49676679	K562	blood:	n/a	n/a
19	MAX	chr10:49674718-49675160	H1-hESC	embryonic stem cell:	n/a	n/a
20	MYC	chr10:49676093-49676744	K562	blood:	n/a	n/a
21	MYC	chr10:49676093-49676742	K562	blood:	n/a	n/a
22	NR2F2	chr10:49676034-49676769	K562	blood:	n/a	n/a
23	NR2F2	chr10:49675707-49676940	K562	blood:	n/a	n/a
24	NRF1	chr10:49674359-49674616	H1-hESC	embryonic stem cell:	n/a	chr10:49674502-49674513 chr10:49674502-49674516 chr10:49674504-49674513
25	PML	chr10:49676041-49676794	K562	blood:	n/a	n/a
26	POLR2A	chr10:49673097-49674061	U87	brain:	n/a	n/a
27	POLR2A	chr10:49673180-49674031	U87	brain:	n/a	n/a
28	POLR2A	chr10:49675855-49679748	K562	blood:	n/a	n/a
29	POLR2A	chr10:49674949-49675561	U87	brain:	n/a	n/a
30	POLR2A	chr10:49676024-49679787	K562	blood:	n/a	n/a
31	POLR2A	chr10:49676037-49676672	K562	blood:	n/a	n/a
32	POLR2A	chr10:49675007-49675508	U87	brain:	n/a	n/a
33	RAD21	chr10:49674862-49675033	H1-hESC	embryonic stem cell:	n/a	n/a
34	RCOR1	chr10:49675931-49676665	K562	blood:	n/a	n/a
35	RCOR1	chr10:49675933-49676675	K562	blood:	n/a	n/a
36	RCOR1	chr10:49675089-49675223	K562	blood:	n/a	n/a
37	RCOR1	chr10:49675044-49675397	K562	blood:	n/a	n/a
38	STAT5A	chr10:49675804-49676717	K562	blood:	n/a	n/a
39	STAT5A	chr10:49676077-49676701	K562	blood:	n/a	n/a
40	TAL1	chr10:49676015-49676791	K562	blood:	n/a	n/a
41	TBL1XR1	chr10:49674980-49675061	K562	blood:	n/a	n/a
42	TBL1XR1	chr10:49676093-49676681	K562	blood:	n/a	n/a
43	TBL1XR1	chr10:49676115-49676689	K562	blood:	n/a	n/a
44	TEAD4	chr10:49674679-49675017	H1-hESC	embryonic stem cell:	n/a	n/a
45	TEAD4	chr10:49676024-49676753	K562	blood:	n/a	n/a
46	TEAD4	chr10:49675940-49676998	K562	blood:	n/a	n/a
47	TEAD4	chr10:49674664-49674946	H1-hESC	embryonic stem cell:	n/a	n/a
48	UBTF	chr10:49675972-49676670	K562	blood:	n/a	n/a
49	ZC3H11A	chr10:49675995-49676029	K562	blood:	n/a	n/a
50	ZMIZ1	chr10:49675981-49676614	K562	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:49674348-49674398	SAEC	small airway:	n/a
2	chr10:49674348-49674398	ProgFib	skin:	n/a
3	chr10:49674530-49674580	HCF	heart:	n/a
4	chr10:49674458-49674508	K562	blood:	n/a
5	chr10:49674251-49674301	GM19239	blood:	n/a
6	chr10:49674348-49674398	HRE	kidney:	n/a
7	chr10:49674251-49674301	PANC-1	pancreas:	n/a
8	chr10:49673534-49673584	NH-A	brain:	n/a
9	chr10:49674530-49674580	NH-A	brain:	n/a
10	chr10:49674251-49674301	ECC-1	luminal epithelium:	n/a
11	chr10:49674348-49674398	K562	blood:	n/a
12	chr10:49674251-49674301	NT2-D1	testis:	n/a
13	chr10:49674348-49674398	Hela-S3	cervix:	n/a
14	chr10:49674251-49674301	CMK	blood:	n/a
15	chr10:49673534-49673584	HCPEpiC	choroid plexus:	n/a
16	chr10:49674883-49674933	PFSK-1	brain:	n/a
17	chr10:49674458-49674508	MCF10A-Er-Src	breast:	n/a
18	chr10:49674530-49674580	Hepatocyte	liver:	n/a
19	chr10:49674348-49674398	GM12892	blood:	n/a
20	chr10:49674458-49674508	AG09309	skin:	n/a
21	chr10:49674251-49674301	HepG2	liver:	n/a
22	chr10:49674883-49674933	SKMC	muscle:	n/a
23	chr10:49673534-49673584	HCT-116	colon:	n/a
24	chr10:49674883-49674933	K562	blood:	n/a
25	chr10:49674251-49674301	MCF-7	breast:	n/a
26	chr10:49674348-49674398	SK-N-MC	brain:	n/a
27	chr10:49674530-49674580	HRPEpiC	eye:	n/a
28	chr10:49674883-49674933	NH-A	brain:	n/a
29	chr10:49674883-49674933	GM19239	blood:	n/a
30	chr10:49673534-49673584	NHBE	bronchial:	n/a
31	chr10:49674458-49674508	SKMC	muscle:	n/a
32	chr10:49673534-49673584	Hepatocyte	liver:	n/a
33	chr10:49674530-49674580	SK-N-SH_RA	brain:	n/a
34	chr10:49673534-49673584	HUVEC	blood vessel:	n/a
35	chr10:49674251-49674301	A549	lung:	n/a
36	chr10:49674348-49674398	HCT-116	colon:	n/a
37	chr10:49674348-49674398	Caco-2	colon:	n/a
38	chr10:49674458-49674508	HCM	heart:	n/a
39	chr10:49674883-49674933	AG04449	skin:	fetal
40	chr10:49674458-49674508	HMEC	breast:	n/a
41	chr10:49674458-49674508	AG10803	skin:	n/a
42	chr10:49674348-49674398	NHDF-neo	bronchial:	n/a
43	chr10:49674251-49674301	ProgFib	skin:	n/a
44	chr10:49673534-49673584	MCF10A-Er-Src	breast:	n/a
45	chr10:49674251-49674301	AG04449	skin:	fetal
46	chr10:49673534-49673584	HPAEpiC	pulmonary alveolar:	n/a
47	chr10:49674530-49674580	HUVEC	blood vessel:	n/a
48	chr10:49674251-49674301	HCF	heart:	n/a
49	chr10:49674458-49674508	HNPCEpiC	eye:	n/a
50	chr10:49674883-49674933	NB4	blood:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:49514501..49516513-chr10:49675847..49678293,2	K562	blood:
2	chr10:49514372..49515875-chr10:49672720..49674716,2	K562	blood:
3	chr10:49639661..49642619-chr10:49674798..49676427,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRMPD2-3	chr10:49676050-49677859	NONHSAT013272

No data

Variant related genes	Relation type
ARHGAP22	TF binding region
ARHGAP22	CpG island
ENSG00000107643	chromatin interactions

Extended variants
information (count: 90 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:90 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561945064	chr10:49673574-49673575	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs376035483	chr10:49673575-49673576	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs529145215	chr10:49673612-49673613	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs147502099	chr10:49673636-49673637	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs559350604	chr10:49673691-49673692	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs532960117	chr10:49673703-49673704	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs139575764	chr10:49673708-49673709	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs143561945	chr10:49673710-49673711	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs537178866	chr10:49673719-49673720	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs61838730	chr10:49673748-49673749	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs568655550	chr10:49673752-49673753	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs535732393	chr10:49673754-49673755	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs147161113	chr10:49673758-49673759	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs537546609	chr10:49673775-49673776	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs572450310	chr10:49673828-49673829	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs188134556	chr10:49673867-49673868	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs557767677	chr10:49673877-49673878	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs113354366	chr10:49673888-49673889	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs576439790	chr10:49673977-49673978	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs543921020	chr10:49673996-49673997	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs561700618	chr10:49674008-49674009	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs573790597	chr10:49674079-49674080	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs112915296	chr10:49674129-49674130	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs540921795	chr10:49674131-49674132	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs559684229	chr10:49674162-49674163	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs370324835	chr10:49674192-49674193	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs533305765	chr10:49674195-49674196	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs544998804	chr10:49674197-49674198	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs563294492	chr10:49674209-49674210	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs530488260	chr10:49674301-49674302	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs200073706	chr10:49674310-49674311	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs5784760	chr10:49674313-49674314	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs373367926	chr10:49674318-49674319	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs549070069	chr10:49674321-49674322	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs372292455	chr10:49674351-49674352	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs116214490	chr10:49674383-49674384	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs73303049	chr10:49674411-49674412	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs4444029	chr10:49674423-49674424	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs547622374	chr10:49674425-49674426	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs566014686	chr10:49674466-49674467	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs111305559	chr10:49674477-49674478	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs180978370	chr10:49674483-49674484	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs4082089	chr10:49674556-49674557	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs377322921	chr10:49674568-49674569	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs570049610	chr10:49674618-49674619	Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs201951264	chr10:49674638-49674639	Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs7922669	chr10:49674641-49674642	Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs1867580	chr10:49674649-49674650	Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs2377352	chr10:49674656-49674657	Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs200260611	chr10:49674658-49674659	Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Schizophrenia	23813976	CNVD
Acute myeloid leukemia	19651601	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Rett syndrome	21593744	CNVD
Glioblastoma multiforme	22286061	CNVD
Neuroblastoma	21899760	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Autism	21948486	CNVD
cleft palate	21948486	CNVD
Encephalopathy	21948486	CNVD
Lung cancer	18438408	CNVD
T-cell primary immunodeficiency	21948486	CNVD
Autism	22543975	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
skeletal anomalies	21948486	CNVD
speech delay	21948486	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:282 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49653000-49673600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr10:49655200-49677800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr10:49657800-49677600	Weak transcription	HSMMtube	muscle
4	chr10:49665400-49675000	Weak transcription	HUVEC	blood vessel
5	chr10:49668200-49674400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr10:49668400-49676200	Weak transcription	NHLF	lung
7	chr10:49668800-49674200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr10:49669000-49674000	Enhancers	K562	blood
9	chr10:49669200-49674800	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr10:49670200-49675200	Weak transcription	Osteobl	bone
11	chr10:49670600-49673600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr10:49670800-49673600	Enhancers	Ovary	ovary
13	chr10:49670800-49674200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr10:49670800-49674800	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr10:49671000-49680400	Enhancers	Primary hematopoietic stem cells	blood
16	chr10:49671200-49673800	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr10:49671200-49674000	Enhancers	Fetal Heart	heart
18	chr10:49671200-49674400	Enhancers	Colon Smooth Muscle	Colon
19	chr10:49671200-49675400	Enhancers	Brain Hippocampus Middle	brain
20	chr10:49671400-49673600	Enhancers	Rectal Smooth Muscle	rectum
21	chr10:49671400-49673800	Enhancers	Brain Cingulate Gyrus	brain
22	chr10:49671400-49673800	Enhancers	Brain Inferior Temporal Lobe	brain
23	chr10:49671400-49673800	Enhancers	Fetal Lung	lung
24	chr10:49671400-49674200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr10:49671400-49674200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr10:49671400-49674200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
27	chr10:49671400-49674800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr10:49671400-49675200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr10:49671400-49675600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr10:49671800-49674200	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr10:49671800-49674400	Enhancers	Esophagus	oesophagus
32	chr10:49672000-49673600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr10:49672200-49674200	Weak transcription	Right Atrium	heart
34	chr10:49672400-49673600	Weak transcription	NHDF-Ad	bronchial
35	chr10:49672400-49674200	Bivalent Enhancer	Fetal Stomach	stomach
36	chr10:49672400-49675200	Bivalent Enhancer	Placenta	Placenta
37	chr10:49672400-49675400	Enhancers	Brain Substantia Nigra	brain
38	chr10:49672400-49677200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr10:49672400-49683400	Weak transcription	Spleen	Spleen
40	chr10:49672600-49673800	Enhancers	Fetal Brain Male	brain
41	chr10:49672600-49674200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr10:49672600-49674200	Bivalent Enhancer	Fetal Muscle Leg	muscle
43	chr10:49672600-49674400	Enhancers	Left Ventricle	heart
44	chr10:49672600-49681800	Weak transcription	Aorta	Aorta
45	chr10:49672800-49674200	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr10:49672800-49674600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr10:49672800-49675200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr10:49673000-49673600	Enhancers	Adipose Nuclei	Adipose
49	chr10:49673000-49674000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
50	chr10:49673000-49681200	Weak transcription	HSMM	muscle

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