Variant report

Variant	rs530329566
Chromosome Location	chr7:6629545-6629546
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TAF1	chr7:6629406-6630102	HepG2	liver:	n/a	n/a
2	POLR2A	chr7:6629245-6630402	GM12878	blood:	n/a	n/a
3	NRF1	chr7:6629084-6630389	SK-N-SH	brain:	n/a	chr7:6629523-6629532
4	GTF2B	chr7:6629523-6629798	K562	blood:	n/a	n/a
5	FOXA1	chr7:6629371-6629885	HepG2	liver:	n/a	n/a
6	MAX	chr7:6629364-6630386	K562	blood:	n/a	n/a
7	CTCF	chr7:6629520-6629670	WERI-Rb-1	eye:	n/a	chr7:6629572-6629582 chr7:6629567-6629585 chr7:6629570-6629583 chr7:6629568-6629584 chr7:6629570-6629579 chr7:6629570-6629583
8	POLR2A	chr7:6628828-6630384	Hela-S3	cervix:	n/a	n/a
9	POLR2A	chr7:6629320-6630101	K562	blood:	n/a	n/a
10	POLR2A	chr7:6629369-6630365	GM15510	blood:	n/a	n/a
11	CTCF	chr7:6629520-6629670	HVMF	connective:	n/a	chr7:6629572-6629582 chr7:6629567-6629585 chr7:6629570-6629583 chr7:6629568-6629584 chr7:6629570-6629579 chr7:6629570-6629583
12	CTCF	chr7:6629540-6629690	GM12874	blood:	n/a	chr7:6629572-6629582 chr7:6629567-6629585 chr7:6629570-6629583 chr7:6629568-6629584 chr7:6629570-6629579 chr7:6629570-6629583
13	POLR2A	chr7:6629383-6629932	HepG2	liver:	n/a	n/a
14	MAX	chr7:6629197-6630487	A549	lung:	n/a	n/a
15	CTCF	chr7:6629520-6629670	NHLF	lung:	n/a	chr7:6629572-6629582 chr7:6629567-6629585 chr7:6629570-6629583 chr7:6629568-6629584 chr7:6629570-6629579 chr7:6629570-6629583
16	POLR2A	chr7:6629325-6630193	GM19099	blood:	n/a	n/a
17	FOSL2	chr7:6629259-6629817	HepG2	liver:	n/a	n/a
18	MXI1	chr7:6629428-6630492	Hela-S3	cervix:	n/a	n/a
19	ZBTB33	chr7:6629384-6629885	A549	lung:	n/a	n/a
20	ARID3A	chr7:6629468-6629712	K562	blood:	n/a	n/a
21	YY1	chr7:6629483-6629670	HCT-116	colon:	n/a	chr7:6629603-6629617 chr7:6629523-6629532
22	HA-E2F1	chr7:6629324-6630258	Hela-S3	cervix:	n/a	chr7:6629523-6629532 chr7:6629776-6629786 chr7:6629734-6629744 chr7:6629720-6629730 chr7:6629673-6629683
23	MAX	chr7:6629362-6630493	NB4	blood:	n/a	n/a
24	POLR2A	chr7:6629317-6630667	MCF10A-Er-Src	breast:	n/a	n/a
25	CTCF	chr7:6629500-6629650	HepG2	liver:	n/a	chr7:6629572-6629582 chr7:6629567-6629585 chr7:6629570-6629583 chr7:6629568-6629584 chr7:6629570-6629579 chr7:6629570-6629583
26	CTCF	chr7:6629520-6629670	GM12875	blood:	n/a	chr7:6629572-6629582 chr7:6629567-6629585 chr7:6629570-6629583 chr7:6629568-6629584 chr7:6629570-6629579 chr7:6629570-6629583
27	PML	chr7:6629524-6629690	GM12878	blood:	n/a	n/a
28	CEBPB	chr7:6629404-6629720	Hela-S3	cervix:	n/a	n/a
29	MYBL2	chr7:6629331-6629852	HepG2	liver:	n/a	n/a
30	ELK1	chr7:6629519-6630135	Hela-S3	cervix:	n/a	n/a
31	RFX5	chr7:6629424-6630453	Hela-S3	cervix:	n/a	n/a
32	ETS1	chr7:6629434-6630072	K562	blood:	n/a	chr7:6629521-6629532 chr7:6629869-6629878 chr7:6629870-6629880
33	TAF1	chr7:6629350-6630016	SK-N-SH	brain:	n/a	n/a
34	CTCF	chr7:6629500-6629650	HPF	lung:	n/a	chr7:6629572-6629582 chr7:6629567-6629585 chr7:6629570-6629583 chr7:6629568-6629584 chr7:6629570-6629579 chr7:6629570-6629583
35	MYC	chr7:6629434-6630004	K562	blood:	n/a	n/a
36	TEAD4	chr7:6629397-6629704	H1-hESC	embryonic stem cell:	n/a	n/a
37	TBL1XR1	chr7:6629455-6629738	K562	blood:	n/a	n/a
38	POLR2A	chr7:6629078-6630303	PANC-1	pancreas:	n/a	n/a
39	RAD21	chr7:6629387-6629763	K562	blood:	n/a	chr7:6629579-6629592 chr7:6629573-6629583 chr7:6629686-6629700 chr7:6629571-6629584 chr7:6629568-6629587 chr7:6629676-6629690
40	NANOG	chr7:6629424-6630042	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr7:6629500-6629650	AG04449	skin:	n/a	chr7:6629572-6629582 chr7:6629567-6629585 chr7:6629570-6629583 chr7:6629568-6629584 chr7:6629570-6629579 chr7:6629570-6629583
42	CTCF	chr7:6629500-6629650	WI-38	lung:	n/a	chr7:6629572-6629582 chr7:6629567-6629585 chr7:6629570-6629583 chr7:6629568-6629584 chr7:6629570-6629579 chr7:6629570-6629583
43	CHD2	chr7:6629242-6629948	H1-hESC	embryonic stem cell:	n/a	chr7:6629561-6629571
44	MAX	chr7:6629369-6630349	ECC-1	luminal epithelium:	n/a	n/a
45	ELF1	chr7:6629412-6629704	HepG2	liver:	n/a	n/a
46	CTCF	chr7:6629410-6629656	ECC-1	luminal epithelium:	n/a	chr7:6629572-6629582 chr7:6629567-6629585 chr7:6629570-6629583 chr7:6629568-6629584 chr7:6629570-6629579 chr7:6629570-6629583
47	TCF3	chr7:6629447-6629781	GM12878	blood:	n/a	n/a
48	ZKSCAN1	chr7:6629423-6629756	Hela-S3	cervix:	n/a	n/a
49	POLR2A	chr7:6629389-6630128	A549	lung:	n/a	n/a
50	YY1	chr7:6629398-6629983	K562	blood:	n/a	chr7:6629733-6629747 chr7:6629798-6629812 chr7:6629603-6629617 chr7:6629698-6629707 chr7:6629779-6629790 chr7:6629523-6629532

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6629515-6629565	MCF-7	breast:	n/a
2	chr7:6629515-6629565	BJ	skin:	n/a
3	chr7:6629515-6629565	HepG2	liver:	n/a
4	chr7:6629515-6629565	RPTEC	kidney:	n/a
5	chr7:6629515-6629565	SAEC	small airway:	n/a
6	chr7:6629515-6629565	NH-A	brain:	n/a
7	chr7:6629515-6629565	AG09309	skin:	n/a
8	chr7:6629515-6629565	HMEC	breast:	n/a
9	chr7:6629515-6629565	AG09319	gingival:	n/a
10	chr7:6629515-6629565	H1-hESC	embryonic stem cell:	embryo
11	chr7:6629515-6629565	HL-60	blood:	n/a
12	chr7:6629515-6629565	ovcar-3	ovarian:	n/a
13	chr7:6629515-6629565	HCT-116	colon:	n/a
14	chr7:6629515-6629565	SK-N-MC	brain:	n/a
15	chr7:6629515-6629565	NHBE	bronchial:	n/a
16	chr7:6629515-6629565	LNCaP	prostate:	n/a
17	chr7:6629515-6629565	A549	lung:	n/a
18	chr7:6629515-6629565	GM19239	blood:	n/a
19	chr7:6629515-6629565	HAEpiC	amniotic membrane:	n/a
20	chr7:6629515-6629565	MCF10A-Er-Src	breast:	n/a
21	chr7:6629515-6629565	Hela-S3	cervix:	n/a
22	chr7:6629515-6629565	HPAEpiC	pulmonary alveolar:	n/a
23	chr7:6629515-6629565	HRPEpiC	eye:	n/a
24	chr7:6629515-6629565	K562	blood:	n/a
25	chr7:6629515-6629565	SKMC	muscle:	n/a
26	chr7:6629515-6629565	PFSK-1	brain:	n/a
27	chr7:6629515-6629565	NT2-D1	testis:	n/a
28	chr7:6629515-6629565	HNPCEpiC	eye:	n/a
29	chr7:6629515-6629565	BE2_C	brain:	n/a
30	chr7:6629515-6629565	ProgFib	skin:	n/a
31	chr7:6629515-6629565	NB4	blood:	n/a
32	chr7:6629515-6629565	GM06990	blood:	n/a
33	chr7:6629515-6629565	GM12891	blood:	n/a
34	chr7:6629515-6629565	HEEpiC	esophagus:	n/a
35	chr7:6629515-6629565	GM12878	blood:	n/a
36	chr7:6629515-6629565	ECC-1	luminal epithelium:	n/a
37	chr7:6629515-6629565	HCF	heart:	n/a
38	chr7:6629515-6629565	Jurkat	blood:	n/a
39	chr7:6629515-6629565	U87	brain:	n/a
40	chr7:6629515-6629565	T-47D	breast:	n/a
41	chr7:6629515-6629565	PANC-1	pancreas:	n/a
42	chr7:6629515-6629565	HIPEpiC	eye:	n/a
43	chr7:6629515-6629565	SK-N-SH_RA	brain:	n/a
44	chr7:6629515-6629565	Hepatocyte	liver:	n/a
45	chr7:6629515-6629565	PrEC	prostate:	n/a
46	chr7:6629515-6629565	HEK293	kidney:	embryo
47	chr7:6629515-6629565	AG04449	skin:	fetal
48	chr7:6629515-6629565	HRE	kidney:	n/a
49	chr7:6629515-6629565	HCM	heart:	n/a
50	chr7:6629515-6629565	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:6523102..6525727-chr7:6628447..6631086,2	MCF-7	breast:
2	chr7:6621445..6626175-chr7:6626576..6631235,7	MCF-7	breast:
3	chr7:6614342..6622557-chr7:6625132..6631922,18	K562	blood:
4	chr17:80250434..80250943-chr7:6629426..6630149,2	HCT-116	colon:
5	chr7:6615687..6618664-chr7:6627812..6632591,8	MCF-7	breast:
6	chr7:6627960..6631587-chr7:6636185..6643600,9	MCF-7	breast:
7	chr7:6628303..6631132-chr7:6637511..6639950,2	K562	blood:
8	chr7:6627001..6634994-chr7:6673643..6681623,15	MCF-7	breast:
9	chr7:6628726..6630315-chr7:6654459..6656349,2	MCF-7	breast:
10	chr7:6628194..6631157-chr7:6744707..6746398,2	MCF-7	breast:
11	chr7:6628215..6631115-chr7:6675239..6679126,9	MCF-7	breast:
12	chr7:6523333..6525416-chr7:6628158..6630053,2	K562	blood:
13	chr7:6626891..6631454-chr7:6676260..6679154,6	K562	blood:
14	chr7:6628238..6630542-chr7:6653702..6656593,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRID2IP-1	chr7:6628988-6629569	NONHSAT119018

Variant related genes	Relation type
ENSG00000232581	TF binding region
C7orf26	TF binding region
ENSG00000232581	CpG island
C7orf26	CpG island
ENSG00000236609	Chromatin interaction
ENSG00000146576	Chromatin interaction
ENSG00000136240	Chromatin interaction
ENSG00000164631	Chromatin interaction
ENSG00000265692	Chromatin interaction
ENSG00000136247	Chromatin interaction
ENSG00000205903	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034060	chr7:5814823-6745710	Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	138 gene(s)	inside rSNPs	diseases
2	nsv538711	chr7:5814823-6745710	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	138 gene(s)	inside rSNPs	diseases
3	nsv1028242	chr7:5819084-6645024	Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS 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	127 gene(s)	inside rSNPs	diseases
4	nsv538712	chr7:5819084-6645024	Weak transcription Active TSS Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	127 gene(s)	inside rSNPs	diseases
5	nsv949531	chr7:5949371-6753694	Strong transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	129 gene(s)	inside rSNPs	diseases
6	nsv1020236	chr7:6248930-6690377	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
7	nsv830895	chr7:6514781-6722092	Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
8	nsv887429	chr7:6520676-6659509	Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
9	nsv887430	chr7:6520676-6668027	Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
10	nsv508444	chr7:6534110-6700527	Bivalent/Poised TSS Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
11	nsv1025220	chr7:6534278-6736802	Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
12	nsv538717	chr7:6534278-6736802	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
13	nsv887431	chr7:6535517-6690240	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
14	nsv515978	chr7:6535517-6698905	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
15	nsv887432	chr7:6535517-6713985	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
16	nsv887433	chr7:6557135-6668027	Enhancers ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
17	nsv887434	chr7:6557135-6713985	Strong transcription Active TSS Genic enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
18	nsv606001	chr7:6563109-6683454	Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
19	nsv606002	chr7:6567114-6713985	Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
20	nsv887435	chr7:6613604-6713985	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
21	nsv824002	chr7:6618087-6716961	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats 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	21 gene(s)	inside rSNPs	diseases
22	nsv824003	chr7:6620920-6721409	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
23	nsv887436	chr7:6626922-6721661	Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
24	esv1797143	chr7:6628177-6705439	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
25	nsv606003	chr7:6628242-6713985	Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
26	esv3381818	chr7:6628877-6630925	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6617600-6629600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:6617600-6629800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr7:6617600-6630000	Weak transcription	Stomach Mucosa	stomach
4	chr7:6624800-6629600	Weak transcription	Aorta	Aorta
5	chr7:6625000-6629800	Weak transcription	Fetal Kidney	kidney
6	chr7:6625000-6629800	Weak transcription	NHDF-Ad	bronchial
7	chr7:6626800-6629600	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr7:6628600-6630400	Active TSS	Rectal Smooth Muscle	rectum
9	chr7:6628800-6629600	Weak transcription	HSMMtube	muscle
10	chr7:6629000-6629600	Weak transcription	Primary T cells from cord blood	blood
11	chr7:6629000-6629600	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr7:6629000-6629600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr7:6629000-6629600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr7:6629000-6629600	Enhancers	Fetal Lung	lung
15	chr7:6629000-6629600	Enhancers	Gastric	stomach
16	chr7:6629000-6629600	Enhancers	Lung	lung
17	chr7:6629000-6629600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
18	chr7:6629000-6629600	Enhancers	Spleen	Spleen
19	chr7:6629000-6629800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr7:6629000-6630400	Active TSS	Brain Germinal Matrix	brain
21	chr7:6629000-6630600	Active TSS	Osteobl	bone
22	chr7:6629000-6630800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr7:6629000-6631000	Active TSS	iPS-15b Cell Line	embryonic stem cell
24	chr7:6629200-6629600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr7:6629200-6629600	Flanking Active TSS	Primary B cells from cord blood	blood
26	chr7:6629200-6629600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
27	chr7:6629200-6629600	Enhancers	Primary hematopoietic stem cells	blood
28	chr7:6629200-6629600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr7:6629200-6629600	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
30	chr7:6629200-6629600	Flanking Active TSS	Colonic Mucosa	Colon
31	chr7:6629200-6629600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
32	chr7:6629200-6629600	Flanking Active TSS	Fetal Muscle Leg	muscle
33	chr7:6629200-6629600	Flanking Active TSS	Thymus	Thymus
34	chr7:6629200-6629600	Flanking Active TSS	Dnd41	blood
35	chr7:6629200-6630400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr7:6629200-6630400	Active TSS	iPS-18 Cell Line	embryonic stem cell
37	chr7:6629200-6630400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr7:6629200-6630400	Active TSS	Colon Smooth Muscle	Colon
39	chr7:6629200-6630400	Active TSS	Fetal Brain Female	brain
40	chr7:6629200-6630400	Active TSS	Hela-S3	cervix
41	chr7:6629200-6630600	Active TSS	ES-I3 Cell Line	embryonic stem cell
42	chr7:6629200-6630600	Active TSS	HUES64 Cell Line	embryonic stem cell
43	chr7:6629200-6630600	Active TSS	iPS-20b Cell Line	embryonic stem cell
44	chr7:6629200-6630600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr7:6629200-6630800	Active TSS	H9 Cell Line	embryonic stem cell
46	chr7:6629200-6630800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr7:6629200-6630800	Active TSS	HUES6 Cell Line	embryonic stem cell
48	chr7:6629200-6630800	Active TSS	Pancreatic Islets	Pancreatic Islet
49	chr7:6629200-6630800	Active TSS	NHLF	lung
50	chr7:6629400-6629600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links