Variant report

Variant	rs17166017
Chromosome Location	chr7:12443390-12443391
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:209)
CpG islands
(count:0)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:209 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TAF7	chr7:12443097-12443851	H1-hESC	embryonic stem cell:	n/a	n/a
2	ARID3A	chr7:12443002-12443779	K562	blood:	n/a	n/a
3	MYC	chr7:12442876-12444310	K562	blood:	n/a	chr7:12443233-12443242
4	CBX3	chr7:12442863-12443396	K562	blood:	n/a	n/a
5	POLR2A	chr7:12442750-12444089	K562	blood:	n/a	n/a
6	POLR2A	chr7:12443057-12443769	Hela-S3	cervix:	n/a	n/a
7	CREB1	chr7:12443283-12443741	A549	lung:	n/a	n/a
8	RCOR1	chr7:12443006-12444411	K562	blood:	n/a	n/a
9	SIN3AK20	chr7:12443054-12443772	PANC-1	pancreas:	n/a	n/a
10	TAF1	chr7:12442780-12443896	K562	blood:	n/a	n/a
11	BACH1	chr7:12443123-12443675	H1-hESC	embryonic stem cell:	n/a	n/a
12	MXI1	chr7:12443071-12443767	K562	blood:	n/a	n/a
13	POLR2A	chr7:12442976-12444516	K562	blood:	n/a	n/a
14	REST	chr7:12443329-12443448	K562	blood:	n/a	n/a
15	CUX1	chr7:12442957-12443842	K562	blood:	n/a	n/a
16	TCF12	chr7:12443125-12443905	ECC-1	luminal epithelium:	n/a	n/a
17	POLR2A	chr7:12443182-12443666	MCF-7	breast:	n/a	n/a
18	NFIC	chr7:12442829-12443573	ECC-1	luminal epithelium:	n/a	n/a
19	JUND	chr7:12443337-12443734	H1-hESC	embryonic stem cell:	n/a	n/a
20	CREB1	chr7:12443080-12443849	H1-hESC	embryonic stem cell:	n/a	n/a
21	TBP	chr7:12443041-12443841	H1-hESC	embryonic stem cell:	n/a	n/a
22	YY1	chr7:12443132-12443733	H1-hESC	embryonic stem cell:	n/a	n/a
23	MAX	chr7:12442915-12444080	A549	lung:	n/a	chr7:12443233-12443242
24	MYC	chr7:12442849-12444429	K562	blood:	n/a	chr7:12443233-12443242
25	CTBP2	chr7:12443038-12444271	H1-hESC	embryonic stem cell:	n/a	n/a
26	MAX	chr7:12442939-12444336	HCT-116	colon:	n/a	chr7:12443233-12443242
27	POLR2A	chr7:12443168-12443649	Hela-S3	cervix:	n/a	n/a
28	ZBTB7A	chr7:12443085-12443506	K562	blood:	n/a	n/a
29	ZKSCAN1	chr7:12442931-12443555	Hela-S3	cervix:	n/a	n/a
30	TCF7L2	chr7:12443066-12444146	Hela-S3	cervix:	n/a	n/a
31	MAX	chr7:12443126-12444171	NB4	blood:	n/a	chr7:12443233-12443242
32	SMC3	chr7:12443129-12443601	K562	blood:	n/a	n/a
33	IRF1	chr7:12442425-12444034	K562	blood:	n/a	n/a
34	MAZ	chr7:12442875-12444216	K562	blood:	n/a	chr7:12443233-12443242
35	TAF7	chr7:12442850-12443464	K562	blood:	n/a	n/a
36	HA-E2F1	chr7:12442913-12444167	MCF-7	breast:	n/a	n/a
37	POLR2A	chr7:12443039-12443891	PANC-1	pancreas:	n/a	n/a
38	TBP	chr7:12442833-12444212	K562	blood:	n/a	n/a
39	GATA2	chr7:12443104-12443505	K562	blood:	n/a	n/a
40	POLR2A	chr7:12443163-12443701	A549	lung:	n/a	n/a
41	POLR2A	chr7:12442849-12444540	K562	blood:	n/a	n/a
42	POLR2A	chr7:12442965-12443869	HCT-116	colon:	n/a	n/a
43	TBL1XR1	chr7:12441607-12444212	K562	blood:	n/a	n/a
44	POLR2A	chr7:12443042-12443902	H1-hESC	embryonic stem cell:	n/a	n/a
45	ZBTB7A	chr7:12443050-12443754	K562	blood:	n/a	n/a
46	SRF	chr7:12443033-12443684	K562	blood:	n/a	n/a
47	MXI1	chr7:12442933-12443765	H1-hESC	embryonic stem cell:	n/a	n/a
48	E2F6	chr7:12443155-12443445	K562	blood:	n/a	n/a
49	POLR2A	chr7:12443170-12443879	NB4	blood:	n/a	n/a
50	POLR2A	chr7:12443201-12443742	H1-hESC	embryonic stem cell:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr20:47537945..47538638-chr7:12442691..12443569,2	Hela-S3	cervix:
2	chr7:12441879..12443410-chr7:12725306..12727318,2	K562	blood:
3	chr7:12441983..12444239-chr7:12724759..12726454,2	K562	blood:

No data

Variant related genes	Relation type
VWDE	TF binding region
ENSG00000122644	Chromatin interaction
ENSG00000271253	Chromatin interaction
ENSG00000124198	Chromatin interaction

Extended variants
information (count: 87 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10085906	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1012462	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1020152	0.95[ASN][1000 genomes]
rs1020153	0.95[ASN][1000 genomes]
rs10215269	0.86[CHB][hapmap]
rs10254572	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10255444	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10266368	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10266592	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10268223	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10278216	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10278300	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10499419	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs1072557	0.88[EUR][1000 genomes]
rs11983017	0.88[EUR][1000 genomes]
rs1440019	0.81[EUR][1000 genomes]
rs1595803	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16877397	0.87[EUR][1000 genomes]
rs16877400	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs16877494	0.86[CHB][hapmap]
rs17165894	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs17165896	0.90[CEU][hapmap]
rs17165906	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs17165910	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs17165936	0.88[EUR][1000 genomes]
rs17165995	0.90[CEU][hapmap];0.86[CHB][hapmap];0.92[JPT][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17166022	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17166028	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17166034	0.81[EUR][1000 genomes]
rs1899031	0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1899034	0.81[JPT][hapmap]
rs2108820	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2159208	0.90[ASN][1000 genomes]
rs28551688	0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35171886	0.87[EUR][1000 genomes]
rs3801366	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs3823844	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs3846989	0.91[ASN][1000 genomes]
rs4719312	0.85[EUR][1000 genomes]
rs4721092	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs4721093	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs4721094	0.85[EUR][1000 genomes]
rs4721095	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs4721099	0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4721104	0.86[CHB][hapmap]
rs57347805	0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs57501786	0.87[EUR][1000 genomes]
rs57623700	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs58280274	0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs58436782	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs58775458	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs59739486	0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs60983130	0.87[EUR][1000 genomes]
rs61529219	0.82[EUR][1000 genomes]
rs66688036	0.82[EUR][1000 genomes]
rs6950922	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6951017	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6959981	0.94[ASN][1000 genomes]
rs6968600	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs6977724	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6977850	0.91[ASN][1000 genomes]
rs73288158	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73288159	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7781993	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7784095	0.87[EUR][1000 genomes]
rs7785791	0.86[CHB][hapmap]
rs7795767	0.88[EUR][1000 genomes]
rs7796334	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7806977	0.87[EUR][1000 genomes]

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

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

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	chr7:12440600-12443400	Active TSS	HUES6 Cell Line	embryonic stem cell
4	chr7:12441200-12443600	Active TSS	H1 Cell Line	embryonic stem cell
5	chr7:12441400-12443800	Active TSS	ES-I3 Cell Line	embryonic stem cell
6	chr7:12441400-12443800	Active TSS	HUES64 Cell Line	embryonic stem cell
7	chr7:12441400-12444200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
8	chr7:12441400-12444200	Active TSS	H9 Cell Line	embryonic stem cell
9	chr7:12441600-12443800	Active TSS	iPS-15b Cell Line	embryonic stem cell
10	chr7:12441800-12443800	Active TSS	HUES48 Cell Line	embryonic stem cell
11	chr7:12442000-12444200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
12	chr7:12442400-12443600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
13	chr7:12442400-12443600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr7:12442400-12443600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr7:12442400-12444000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr7:12442400-12444400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
17	chr7:12442600-12443400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
18	chr7:12442600-12443400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr7:12442600-12443800	Active TSS	Primary T cells from cord blood	blood
20	chr7:12442600-12443800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
21	chr7:12442600-12443800	Bivalent/Poised TSS	A549	lung
22	chr7:12442600-12443800	Active TSS	GM12878-XiMat	blood
23	chr7:12442600-12444000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr7:12442600-12444000	Active TSS	Primary T helper naive cells fromperipheralblood	blood
25	chr7:12442600-12444000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
26	chr7:12442600-12444000	Active TSS	Brain Angular Gyrus	brain
27	chr7:12442600-12444000	Active TSS	Hela-S3	cervix
28	chr7:12442600-12444200	Active TSS	Brain Anterior Caudate	brain
29	chr7:12442800-12443400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
30	chr7:12442800-12443400	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
31	chr7:12442800-12443400	Flanking Active TSS	Fetal Brain Female	brain
32	chr7:12442800-12443400	Bivalent/Poised TSS	Osteobl	bone
33	chr7:12442800-12443600	Active TSS	Primary hematopoietic stem cells	blood
34	chr7:12442800-12443600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
35	chr7:12442800-12443600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
36	chr7:12442800-12443600	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr7:12442800-12443600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
38	chr7:12442800-12443800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr7:12442800-12443800	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr7:12442800-12443800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr7:12442800-12443800	Bivalent/Poised TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr7:12442800-12443800	Active TSS	Breast Myoepithelial Primary Cells	Breast
43	chr7:12442800-12443800	Enhancers	Primary B cells from peripheral blood	blood
44	chr7:12442800-12443800	Active TSS	Primary T helper naive cells from peripheral blood	blood
45	chr7:12442800-12443800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
46	chr7:12442800-12443800	Active TSS	Fetal Kidney	kidney
47	chr7:12442800-12444000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr7:12442800-12444000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr7:12442800-12444000	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
50	chr7:12442800-12444000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain

The 2.0 version of rSNPBase

Variant report

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