Variant report

Variant	rs6968600
Chromosome Location	chr7:12444013-12444014
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:70)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:70 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MYC	chr7:12442876-12444310	K562	blood:	n/a	chr7:12443233-12443242
2	POLR2A	chr7:12442750-12444089	K562	blood:	n/a	n/a
3	RCOR1	chr7:12443006-12444411	K562	blood:	n/a	n/a
4	POLR2A	chr7:12442976-12444516	K562	blood:	n/a	n/a
5	MYC	chr7:12443901-12444206	H1-hESC	embryonic stem cell:	n/a	n/a
6	MAX	chr7:12443855-12444295	H1-hESC	embryonic stem cell:	n/a	n/a
7	MAX	chr7:12442915-12444080	A549	lung:	n/a	chr7:12443233-12443242
8	MYC	chr7:12442849-12444429	K562	blood:	n/a	chr7:12443233-12443242
9	CTBP2	chr7:12443038-12444271	H1-hESC	embryonic stem cell:	n/a	n/a
10	MAX	chr7:12442939-12444336	HCT-116	colon:	n/a	chr7:12443233-12443242
11	TCF7L2	chr7:12443066-12444146	Hela-S3	cervix:	n/a	n/a
12	MAX	chr7:12443126-12444171	NB4	blood:	n/a	chr7:12443233-12443242
13	IRF1	chr7:12442425-12444034	K562	blood:	n/a	n/a
14	MAZ	chr7:12442875-12444216	K562	blood:	n/a	chr7:12443233-12443242
15	HA-E2F1	chr7:12442913-12444167	MCF-7	breast:	n/a	n/a
16	TBP	chr7:12442833-12444212	K562	blood:	n/a	n/a
17	POLR2A	chr7:12442849-12444540	K562	blood:	n/a	n/a
18	TBL1XR1	chr7:12441607-12444212	K562	blood:	n/a	n/a
19	MAX	chr7:12442884-12444453	K562	blood:	n/a	chr7:12443233-12443242
20	TCF7L2	chr7:12443198-12444057	PANC-1	pancreas:	n/a	n/a
21	TBL1XR1	chr7:12442792-12444242	K562	blood:	n/a	n/a
22	MAX	chr7:12442961-12444232	K562	blood:	n/a	chr7:12443233-12443242
23	HEY1	chr7:12442781-12444028	K562	blood:	n/a	n/a
24	POLR2A	chr7:12442875-12444428	K562	blood:	n/a	n/a
25	MAX	chr7:12442804-12444100	ECC-1	luminal epithelium:	n/a	chr7:12443233-12443242
26	POLR2A	chr7:12442779-12444617	K562	blood:	n/a	n/a
27	JUND	chr7:12442886-12444171	K562	blood:	n/a	n/a
28	MYC	chr7:12442974-12444192	K562	blood:	n/a	chr7:12443233-12443242
29	KAP1	chr7:12442696-12444041	HEK293	kidney:	n/a	n/a
30	MAX	chr7:12442718-12444384	HCT-116	colon:	n/a	chr7:12443233-12443242
31	STAT5A	chr7:12442779-12444099	K562	blood:	n/a	chr7:12443545-12443557
32	ATF1	chr7:12442940-12444036	K562	blood:	n/a	n/a
33	MYC	chr7:12442984-12444280	K562	blood:	n/a	chr7:12443233-12443242
34	POLR2A	chr7:12442500-12444710	K562	blood:	n/a	n/a
35	MAX	chr7:12443856-12444215	H1-hESC	embryonic stem cell:	n/a	n/a
36	ZC3H11A	chr7:12443362-12444107	K562	blood:	n/a	n/a
37	CEBPB	chr7:12443418-12444101	K562	blood:	n/a	n/a
38	HEY1	chr7:12442863-12444110	K562	blood:	n/a	n/a
39	GTF2B	chr7:12443294-12444017	K562	blood:	n/a	n/a
40	RCOR1	chr7:12442854-12444198	K562	blood:	n/a	n/a
41	MXI1	chr7:12442243-12444388	SK-N-SH	brain:	n/a	n/a
42	TRIM28	chr7:12442743-12444111	K562	blood:	n/a	n/a
43	POLR2A	chr7:12442824-12444072	K562	blood:	n/a	n/a
44	REST	chr7:12443042-12444129	K562	blood:	n/a	n/a
45	MYC	chr7:12442775-12444425	K562	blood:	n/a	chr7:12443233-12443242
46	POLR2A	chr7:12442749-12444633	K562	blood:	n/a	n/a
47	POLR2A	chr7:12442876-12444136	K562	blood:	n/a	n/a
48	POLR2A	chr7:12442747-12444124	H1-hESC	embryonic stem cell:	n/a	n/a
49	TCF7L2	chr7:12442907-12444085	HCT-116	colon:	n/a	n/a
50	HCFC1	chr7:12443004-12444063	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:12444013-12444063	HIPEpiC	eye:	n/a
2	chr7:12444013-12444063	MCF10A-Er-Src	breast:	n/a
3	chr7:12444013-12444063	K562	blood:	n/a
4	chr7:12444013-12444063	HEK293	kidney:	embryo
5	chr7:12444013-12444063	SAEC	small airway:	n/a
6	chr7:12444013-12444063	BJ	skin:	n/a
7	chr7:12444013-12444063	GM12891	blood:	n/a
8	chr7:12444013-12444063	HRCEpiC	kidney:	n/a
9	chr7:12444013-12444063	A549	lung:	n/a
10	chr7:12444013-12444063	HL-60	blood:	n/a
11	chr7:12444013-12444063	ProgFib	skin:	n/a
12	chr7:12444013-12444063	AG04449	skin:	fetal
13	chr7:12444013-12444063	HCT-116	colon:	n/a
14	chr7:12444013-12444063	BE2_C	brain:	n/a
15	chr7:12444013-12444063	NHDF-neo	bronchial:	n/a
16	chr7:12444013-12444063	AG09309	skin:	n/a
17	chr7:12444013-12444063	GM12878	blood:	n/a
18	chr7:12444013-12444063	HUVEC	blood vessel:	n/a
19	chr7:12444013-12444063	Hepatocyte	liver:	n/a
20	chr7:12444013-12444063	AG10803	skin:	n/a
21	chr7:12444013-12444063	U87	brain:	n/a
22	chr7:12444013-12444063	PrEC	prostate:	n/a
23	chr7:12444013-12444063	SK-N-SH_RA	brain:	n/a
24	chr7:12444013-12444063	AoSMC	blood vessel:	n/a
25	chr7:12444013-12444063	NB4	blood:	n/a
26	chr7:12444013-12444063	HAEpiC	amniotic membrane:	n/a
27	chr7:12444013-12444063	GM19239	blood:	n/a
28	chr7:12444013-12444063	NHBE	bronchial:	n/a
29	chr7:12444013-12444063	AG09319	gingival:	n/a
30	chr7:12444013-12444063	Hela-S3	cervix:	n/a
31	chr7:12444013-12444063	MCF-7	breast:	n/a
32	chr7:12444013-12444063	SK-N-MC	brain:	n/a
33	chr7:12444013-12444063	H1-hESC	embryonic stem cell:	embryo
34	chr7:12444013-12444063	HCM	heart:	n/a
35	chr7:12444013-12444063	SK-N-SH	brain:	n/a
36	chr7:12444013-12444063	NT2-D1	testis:	n/a
37	chr7:12444013-12444063	NH-A	brain:	n/a
38	chr7:12444013-12444063	Jurkat	blood:	n/a
39	chr7:12444013-12444063	HMEC	breast:	n/a
40	chr7:12444013-12444063	ECC-1	luminal epithelium:	n/a
41	chr7:12444013-12444063	ovcar-3	ovarian:	n/a
42	chr7:12444013-12444063	HRE	kidney:	n/a
43	chr7:12444013-12444063	Caco-2	colon:	n/a
44	chr7:12444013-12444063	T-47D	breast:	n/a
45	chr7:12444013-12444063	PANC-1	pancreas:	n/a
46	chr7:12444013-12444063	HCPEpiC	choroid plexus:	n/a
47	chr7:12444013-12444063	RPTEC	kidney:	n/a
48	chr7:12444013-12444063	GM06990	blood:	n/a
49	chr7:12444013-12444063	HepG2	liver:	n/a
50	chr7:12444013-12444063	HPAEpiC	pulmonary alveolar:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:12441983..12444239-chr7:12724759..12726454,2	K562	blood:
2	chr7:12414352..12417133-chr7:12443944..12445537,2	K562	blood:

No data

Variant related genes	Relation type
VWDE	TF binding region
VWDE	CpG island
ENSG00000271253	Chromatin interaction

Extended variants
information (count: 123 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:105)

rs_ID	r²[population]
rs10085906	1.00[CHB][hapmap];0.92[JPT][hapmap];0.95[ASN][1000 genomes]
rs1012462	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs1020152	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1020153	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10215269	0.86[CHB][hapmap];0.87[CHD][hapmap];0.91[GIH][hapmap];0.81[TSI][hapmap]
rs10254572	1.00[CHB][hapmap];1.00[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs10255444	0.99[ASN][1000 genomes]
rs10266368	0.95[ASN][1000 genomes]
rs10266592	0.99[ASN][1000 genomes]
rs10268223	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.99[ASN][1000 genomes]
rs10276892	0.83[EUR][1000 genomes]
rs10278216	1.00[CHB][hapmap];0.92[JPT][hapmap];0.95[ASN][1000 genomes]
rs10278300	1.00[CHB][hapmap];0.92[JPT][hapmap];0.95[ASN][1000 genomes]
rs10488159	0.86[EUR][1000 genomes]
rs1371606	0.88[EUR][1000 genomes]
rs1371607	0.88[EUR][1000 genomes]
rs1440024	0.82[EUR][1000 genomes]
rs1595803	0.95[ASN][1000 genomes]
rs16877494	0.86[CHB][hapmap]
rs17165929	0.94[CEU][hapmap];0.81[EUR][1000 genomes]
rs17165934	0.81[EUR][1000 genomes]
rs17165942	0.82[EUR][1000 genomes]
rs17165995	0.86[CHB][hapmap];1.00[CHD][hapmap];0.92[JPT][hapmap];0.86[YRI][hapmap];0.95[ASN][1000 genomes]
rs17166017	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs17166022	0.95[ASN][1000 genomes]
rs17166028	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs17190390	0.82[EUR][1000 genomes]
rs17275374	0.82[EUR][1000 genomes]
rs17275416	0.82[EUR][1000 genomes]
rs17275527	0.82[EUR][1000 genomes]
rs17444465	0.86[EUR][1000 genomes]
rs17444621	0.86[EUR][1000 genomes]
rs17444773	0.86[EUR][1000 genomes]
rs17445017	0.81[EUR][1000 genomes]
rs17541429	0.88[EUR][1000 genomes]
rs17542082	0.86[EUR][1000 genomes]
rs17542109	0.86[EUR][1000 genomes]
rs17542227	0.86[EUR][1000 genomes]
rs17542243	0.86[EUR][1000 genomes]
rs1899031	0.99[ASN][1000 genomes]
rs1899034	0.89[CEU][hapmap];0.81[JPT][hapmap];0.86[MEX][hapmap];0.88[EUR][1000 genomes]
rs2016299	0.86[EUR][1000 genomes]
rs2108820	0.86[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2119141	0.85[MEX][hapmap]
rs2159208	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28551688	0.97[ASN][1000 genomes]
rs3846989	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4719312	0.82[ASN][1000 genomes]
rs4721099	0.90[ASN][1000 genomes]
rs4721104	0.86[CHB][hapmap]
rs56816811	0.86[EUR][1000 genomes]
rs57173744	0.84[EUR][1000 genomes]
rs57347805	0.90[ASN][1000 genomes]
rs57623700	0.99[ASN][1000 genomes]
rs57682619	0.86[EUR][1000 genomes]
rs58280274	0.90[ASN][1000 genomes]
rs58436782	0.96[ASN][1000 genomes]
rs58775458	0.95[ASN][1000 genomes]
rs59681520	0.86[EUR][1000 genomes]
rs59739486	0.96[ASN][1000 genomes]
rs59867765	0.86[EUR][1000 genomes]
rs61240945	0.86[EUR][1000 genomes]
rs62447605	0.86[EUR][1000 genomes]
rs62447606	0.85[EUR][1000 genomes]
rs62447630	0.86[EUR][1000 genomes]
rs62447631	0.86[EUR][1000 genomes]
rs62447632	0.86[EUR][1000 genomes]
rs62447635	0.86[EUR][1000 genomes]
rs62448569	0.81[EUR][1000 genomes]
rs62448622	0.86[EUR][1000 genomes]
rs62448624	0.86[EUR][1000 genomes]
rs62448625	0.88[EUR][1000 genomes]
rs6460937	0.94[CEU][hapmap];0.81[EUR][1000 genomes]
rs6460940	0.81[EUR][1000 genomes]
rs6945357	0.81[EUR][1000 genomes]
rs6950922	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs6951017	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs6959981	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6977724	0.96[ASN][1000 genomes]
rs6977850	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73288158	0.96[ASN][1000 genomes]
rs73288159	0.92[ASN][1000 genomes]
rs7781993	1.00[CHB][hapmap];0.92[JPT][hapmap];0.94[ASN][1000 genomes]
rs7783806	0.86[EUR][1000 genomes]
rs7785791	0.86[CHB][hapmap]
rs7785905	0.82[EUR][1000 genomes]
rs7789937	0.94[CEU][hapmap];0.84[MEX][hapmap];0.90[TSI][hapmap];0.83[EUR][1000 genomes]
rs7790957	0.86[EUR][1000 genomes]
rs7791259	0.82[EUR][1000 genomes]
rs7795767	0.82[ASN][1000 genomes]
rs7796334	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs7796561	0.81[EUR][1000 genomes]
rs7796884	0.94[CEU][hapmap];0.81[EUR][1000 genomes]
rs7797283	0.94[CEU][hapmap];0.83[GIH][hapmap];0.93[MEX][hapmap];0.87[TSI][hapmap];0.81[EUR][1000 genomes]
rs7802736	0.81[EUR][1000 genomes]
rs847908	0.87[AFR][1000 genomes]
rs847909	0.87[AFR][1000 genomes]
rs847910	0.87[AFR][1000 genomes]
rs847989	0.88[AFR][1000 genomes]
rs848001	0.86[YRI][hapmap]
rs887067	0.86[EUR][1000 genomes]
rs920428	0.86[EUR][1000 genomes]
rs920429	0.84[EUR][1000 genomes]
rs920430	0.86[EUR][1000 genomes]
rs970035	0.88[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv606199	chr7:11506143-12486659	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv534432	chr7:12148960-12693032	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv1024554	chr7:12214722-12967418	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
4	nsv538735	chr7:12214722-12967418	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
5	nsv1029941	chr7:12351595-12444490	Flanking Bivalent TSS/Enh Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv1034475	chr7:12352210-12444490	Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv464373	chr7:12406826-12536336	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv606224	chr7:12406826-12536336	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv887635	chr7:12410112-12474635	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
10	nsv887636	chr7:12424405-12498138	Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
11	nsv887637	chr7:12424405-12508894	Enhancers Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
12	nsv887638	chr7:12424405-12519212	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
13	nsv464375	chr7:12428803-12505373	Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
14	nsv606226	chr7:12428803-12505373	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
15	nsv464376	chr7:12429488-12526282	Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
16	nsv606227	chr7:12429488-12526282	Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
17	nsv971508	chr7:12431973-12446365	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
18	nsv516511	chr7:12439672-12479584	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs6968600	VWDE	cis	Thyroid	GTEx
rs6968600	CDYL2	trans	parietal	SCAN

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12438800-12445400	Active TSS	K562	blood
2	chr7:12439600-12444400	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr7:12441400-12444200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
4	chr7:12441400-12444200	Active TSS	H9 Cell Line	embryonic stem cell
5	chr7:12442000-12444200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
6	chr7:12442400-12444400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
7	chr7:12442600-12444200	Active TSS	Brain Anterior Caudate	brain
8	chr7:12442800-12444200	Active TSS	Primary T killer memory cells from peripheral blood	blood
9	chr7:12442800-12444200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr7:12442800-12444200	Active TSS	Brain Inferior Temporal Lobe	brain
11	chr7:12443200-12444200	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
12	chr7:12443400-12444400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
13	chr7:12443600-12444200	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
14	chr7:12443600-12444200	Flanking Active TSS	Primary hematopoietic stem cells	blood
15	chr7:12443600-12444200	Active TSS	Rectal Mucosa Donor 29	rectum
16	chr7:12443600-12444400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr7:12443600-12444600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr7:12443600-12444600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr7:12443800-12444200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
20	chr7:12443800-12444200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
21	chr7:12443800-12444400	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr7:12443800-12444400	Enhancers	Esophagus	oesophagus
23	chr7:12443800-12444400	Enhancers	Lung	lung
24	chr7:12443800-12444400	Active TSS	A549	lung
25	chr7:12443800-12444600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
26	chr7:12443800-12444600	Enhancers	Gastric	stomach
27	chr7:12444000-12444200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
28	chr7:12444000-12444200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
29	chr7:12444000-12444200	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr7:12444000-12444200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
31	chr7:12444000-12444200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
32	chr7:12444000-12444200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr7:12444000-12444200	Enhancers	Brain Hippocampus Middle	brain
34	chr7:12444000-12444200	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
35	chr7:12444000-12444400	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr7:12444000-12444400	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr7:12444000-12444400	Enhancers	Placenta	Placenta
38	chr7:12444000-12444400	Bivalent Enhancer	HepG2	liver
39	chr7:12444000-12444400	Enhancers	HMEC	breast
40	chr7:12444000-12444400	Active TSS	Monocytes-CD14+_RO01746	blood
41	chr7:12444000-12444600	Enhancers	Breast Myoepithelial Primary Cells	Breast

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