Variant report

Variant	rs9972481
Chromosome Location	chr15:77926536-77926537
allele	A/G
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	TCF12	chr15:77926244-77926550	H1-hESC	embryonic stem cell:	n/a	n/a
2	SMC3	chr15:77925473-77927244	SK-N-SH	brain:	n/a	chr15:77925870-77925880 chr15:77925948-77925962 chr15:77925912-77925922 chr15:77926954-77926964 chr15:77926950-77926958 chr15:77926950-77926964 chr15:77926007-77926021
3	ZNF263	chr15:77923899-77927072	HEK293-T-REx	kidney:	n/a	chr15:77924758-77924767 chr15:77926052-77926061 chr15:77925322-77925331 chr15:77926338-77926347
4	RAD21	chr15:77925740-77927127	H1-hESC	embryonic stem cell:	n/a	chr15:77926011-77926021 chr15:77925950-77925963 chr15:77926006-77926025 chr15:77926949-77926968 chr15:77926952-77926965 chr15:77925952-77925964 chr15:77926007-77926021 chr15:77925947-77925966 chr15:77925870-77925880 chr15:77926009-77926022 chr15:77925994-77926008 chr15:77926954-77926964 chr15:77926011-77926023
5	ZNF263	chr15:77924464-77926639	K562	blood:	n/a	chr15:77924758-77924767 chr15:77926052-77926061 chr15:77925322-77925331 chr15:77926338-77926347
6	GTF2F1	chr15:77925850-77926594	H1-hESC	embryonic stem cell:	n/a	n/a
7	MXI1	chr15:77925637-77926993	H1-hESC	embryonic stem cell:	n/a	n/a
8	YY1	chr15:77925725-77927051	H1-hESC	embryonic stem cell:	n/a	chr15:77926548-77926559
9	MXI1	chr15:77925361-77926571	IMR90	lung:	n/a	n/a
10	CTCF	chr15:77925217-77927134	HCT-116	colon:	n/a	chr15:77926005-77926023 chr15:77925949-77925962 chr15:77925947-77925963 chr15:77926008-77926021 chr15:77926951-77926960 chr15:77926948-77926966 chr15:77926950-77926971 chr15:77925946-77925964 chr15:77925948-77925969 chr15:77926951-77926964 chr15:77926007-77926028 chr15:77926344-77926353
11	TEAD4	chr15:77925695-77927069	H1-hESC	embryonic stem cell:	n/a	n/a
12	ZNF143	chr15:77925145-77927535	H1-hESC	embryonic stem cell:	n/a	chr15:77925310-77925328 chr15:77927084-77927103 chr15:77927155-77927173 chr15:77926483-77926501
13	MAX	chr15:77925072-77926605	H1-hESC	embryonic stem cell:	n/a	chr15:77925671-77925678 chr15:77926530-77926539 chr15:77926409-77926419
14	CHD2	chr15:77925542-77927058	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTBP2	chr15:77925487-77927481	H1-hESC	embryonic stem cell:	n/a	n/a
16	TEAD4	chr15:77925733-77927104	H1-hESC	embryonic stem cell:	n/a	n/a
17	SIN3A	chr15:77925513-77927021	H1-hESC	embryonic stem cell:	n/a	chr15:77926561-77926569
18	CTCF	chr15:77926460-77926610	HEEpiC	esophagus:	n/a	n/a
19	JUND	chr15:77925811-77926924	H1-hESC	embryonic stem cell:	n/a	n/a
20	SP1	chr15:77925692-77926695	H1-hESC	embryonic stem cell:	n/a	chr15:77925924-77925936 chr15:77926415-77926424 chr15:77926550-77926559 chr15:77926411-77926425 chr15:77925926-77925935
21	SP1	chr15:77925857-77926651	H1-hESC	embryonic stem cell:	n/a	chr15:77925924-77925936 chr15:77926415-77926424 chr15:77926550-77926559 chr15:77926411-77926425 chr15:77925926-77925935
22	CTCF	chr15:77926500-77926650	RPTEC	kidney:	n/a	n/a
23	CTCF	chr15:77924998-77927629	SK-N-SH	brain:	n/a	chr15:77926005-77926023 chr15:77925949-77925962 chr15:77925947-77925963 chr15:77926008-77926021 chr15:77926951-77926960 chr15:77926948-77926966 chr15:77926950-77926971 chr15:77925946-77925964 chr15:77925948-77925969 chr15:77926951-77926964 chr15:77926007-77926028 chr15:77926344-77926353
24	CREB1	chr15:77925792-77926741	H1-hESC	embryonic stem cell:	n/a	n/a
25	RAD21	chr15:77925015-77926561	SK-N-SH	brain:	n/a	chr15:77926011-77926021 chr15:77925950-77925963 chr15:77926006-77926025 chr15:77925952-77925964 chr15:77926007-77926021 chr15:77925947-77925966 chr15:77925870-77925880 chr15:77926009-77926022 chr15:77925994-77926008 chr15:77926011-77926023
26	RAD21	chr15:77925667-77927188	H1-hESC	embryonic stem cell:	n/a	chr15:77926011-77926021 chr15:77925950-77925963 chr15:77926006-77926025 chr15:77926949-77926968 chr15:77926952-77926965 chr15:77925952-77925964 chr15:77926007-77926021 chr15:77925947-77925966 chr15:77925870-77925880 chr15:77926009-77926022 chr15:77925994-77926008 chr15:77926954-77926964 chr15:77926011-77926023
27	POLR2A	chr15:77925097-77927030	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr15:77925461-77927008	H1-hESC	embryonic stem cell:	n/a	n/a
29	TCF12	chr15:77925854-77926693	H1-hESC	embryonic stem cell:	n/a	chr15:77926169-77926179 chr15:77925956-77925966
30	KAP1	chr15:77925621-77926917	HEK293	kidney:	n/a	n/a
31	POU5F1	chr15:77926053-77926649	H1-hESC	embryonic stem cell:	n/a	chr15:77926362-77926376
32	CTCF	chr15:77926513-77926712	GM12891	blood:	n/a	n/a
33	CTCF	chr15:77925120-77927959	A549	lung:	n/a	chr15:77926005-77926023 chr15:77925949-77925962 chr15:77925947-77925963 chr15:77926008-77926021 chr15:77926951-77926960 chr15:77926948-77926966 chr15:77926950-77926971 chr15:77925946-77925964 chr15:77925948-77925969 chr15:77926951-77926964 chr15:77926007-77926028 chr15:77926344-77926353
34	NANOG	chr15:77925805-77926566	H1-hESC	embryonic stem cell:	n/a	chr15:77926346-77926355
35	CTCF	chr15:77926520-77926670	AG04450	lung:	n/a	n/a
36	CTCF	chr15:77926480-77926630	BJ	skin:	n/a	n/a
37	MYC	chr15:77925528-77926693	H1-hESC	embryonic stem cell:	n/a	chr15:77925671-77925678 chr15:77926530-77926539 chr15:77926409-77926419
38	HDAC2	chr15:77925749-77926542	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr15:77926484-77926716	GM12878	blood:	n/a	n/a
40	ATF2	chr15:77925762-77927046	H1-hESC	embryonic stem cell:	n/a	n/a
41	REST	chr15:77922878-77926930	H1-neurons	neurons:	n/a	chr15:77924598-77924618 chr15:77925405-77925418 chr15:77926562-77926570 chr15:77923211-77923231 chr15:77924598-77924618 chr15:77925784-77925793 chr15:77923269-77923282 chr15:77924408-77924418 chr15:77924761-77924774 chr15:77924598-77924618 chr15:77926406-77926419 chr15:77924348-77924361 chr15:77923214-77923227 chr15:77925893-77925906
42	TBP	chr15:77925758-77927057	H1-hESC	embryonic stem cell:	n/a	n/a
43	MAX	chr15:77925178-77926561	H1-hESC	embryonic stem cell:	n/a	chr15:77925671-77925678 chr15:77926530-77926539 chr15:77926409-77926419
44	CREB1	chr15:77925694-77927515	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr15:77925384-77927145	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr15:77926400-77926550	HMEC	breast:	n/a	n/a
47	TCF12	chr15:77925273-77927049	A549	lung:	n/a	chr15:77926169-77926179 chr15:77926948-77926958 chr15:77925956-77925966
48	MAX	chr15:77925475-77926892	H1-hESC	embryonic stem cell:	n/a	chr15:77925671-77925678 chr15:77926530-77926539 chr15:77926409-77926419
49	RAD21	chr15:77925516-77927094	HCT-116	colon:	n/a	chr15:77926011-77926021 chr15:77925950-77925963 chr15:77926006-77926025 chr15:77926949-77926968 chr15:77926952-77926965 chr15:77925952-77925964 chr15:77926007-77926021 chr15:77925947-77925966 chr15:77925870-77925880 chr15:77926009-77926022 chr15:77925994-77926008 chr15:77926954-77926964 chr15:77926011-77926023
50	CTCF	chr15:77926520-77926670	NHLF	lung:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:77925249..77927257-chr15:78113205..78115049,24	MCF-7	breast:
2	chr15:77925299..77927652-chr15:78112444..78114100,3	MCF-7	breast:
3	chr15:77925435..77927439-chr15:78112259..78115090,22	K562	blood:
4	chr15:77923251..77928296-chr15:78111448..78115771,8	MCF-7	breast:
5	chr15:77924601..77927275-chr15:77937272..77938910,2	K562	blood:
6	chr15:77925397..77928069-chr15:78112259..78116246,3	K562	blood:
7	chr15:77925072..77927787-chr15:78111223..78115888,59	MCF-7	breast:
8	chr15:77924941..77926828-chr15:77932359..77934227,2	MCF-7	breast:
9	chr15:77925397..77927315-chr15:78112259..78115116,2	K562	blood:

Variant related genes	Relation type
LINGO1	TF binding region
ENSG00000259666	Chromatin interaction
ENSG00000169783	Chromatin interaction

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs11072660	0.87[LWK][hapmap];0.81[MKK][hapmap];0.85[YRI][hapmap]
rs11630768	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11633639	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.88[TSI][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11634778	0.83[CHB][hapmap];0.86[JPT][hapmap];0.87[ASN][1000 genomes]
rs11635239	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11638318	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11854903	0.83[AFR][1000 genomes]
rs11855155	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.88[TSI][hapmap];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11856978	0.90[CHB][hapmap];0.81[YRI][hapmap]
rs11857045	0.91[CHB][hapmap]
rs13329256	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.88[TSI][hapmap];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13329323	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16969027	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.88[TSI][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1877292	0.86[JPT][hapmap]
rs1877294	0.83[CHB][hapmap];0.91[GIH][hapmap];0.81[JPT][hapmap]
rs1877295	0.83[CHB][hapmap];0.81[JPT][hapmap]
rs1877298	1.00[CEU][hapmap];0.90[CHB][hapmap];0.81[JPT][hapmap];0.85[YRI][hapmap];0.83[AFR][1000 genomes]
rs1995972	0.83[AFR][1000 genomes]
rs2292415	0.85[CEU][hapmap];0.91[CHB][hapmap];0.93[JPT][hapmap];0.88[TSI][hapmap];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2292416	0.85[CEU][hapmap];0.91[CHB][hapmap];0.93[JPT][hapmap];0.88[TSI][hapmap];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2292417	0.85[CEU][hapmap];0.91[CHB][hapmap];0.93[JPT][hapmap];0.88[TSI][hapmap];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28374408	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28503184	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28515899	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28649029	0.81[AFR][1000 genomes]
rs56717248	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56941158	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60886924	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7165679	0.83[CHB][hapmap];0.91[GIH][hapmap];0.81[JPT][hapmap]
rs7171716	0.91[CHB][hapmap];0.81[JPT][hapmap]
rs74025333	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs74025334	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74025342	0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs74025352	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8024724	0.91[CHB][hapmap]
rs8024932	0.83[CHB][hapmap];0.86[GIH][hapmap]
rs8026164	0.83[CHB][hapmap];0.81[JPT][hapmap]
rs8026671	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8027456	0.91[CHB][hapmap]
rs8028788	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9652488	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9806280	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9920101	0.83[CHB][hapmap];0.86[GIH][hapmap];0.81[JPT][hapmap]
rs9920113	0.91[CHB][hapmap]
rs9920127	0.83[CHB][hapmap];0.91[GIH][hapmap];0.81[JPT][hapmap]
rs9920132	0.94[ASW][hapmap];0.90[GIH][hapmap];0.81[JPT][hapmap];0.80[LWK][hapmap];0.82[YRI][hapmap]
rs9920134	0.91[CHB][hapmap]
rs9920869	0.83[CHB][hapmap];0.80[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1040852	chr15:77160237-78137541	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv916323	chr15:77485765-78121259	Enhancers Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS 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	29 gene(s)	inside rSNPs	diseases
3	nsv833060	chr15:77816654-78035204	Weak transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	esv1806097	chr15:77817889-78301377	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
5	nsv904415	chr15:77845959-77943935	Weak transcription Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv904416	chr15:77845959-77967416	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Strong transcription 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	nsv904417	chr15:77851535-77935992	Weak transcription Flanking Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv904418	chr15:77851535-77963887	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv904419	chr15:77897197-77943935	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	esv3355911	chr15:77924122-77926670	Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:77923000-77927400	Active TSS	HUES48 Cell Line	embryonic stem cell
2	chr15:77923400-77927600	Active TSS	H9 Cell Line	embryonic stem cell
3	chr15:77923600-77926600	Active TSS	iPS-15b Cell Line	embryonic stem cell
4	chr15:77924000-77927600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr15:77924400-77926600	Active TSS	H1 Cell Line	embryonic stem cell
6	chr15:77924400-77926600	Active TSS	iPS-18 Cell Line	embryonic stem cell
7	chr15:77924600-77926600	Active TSS	iPS-20b Cell Line	embryonic stem cell
8	chr15:77924600-77927000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
9	chr15:77924600-77927400	Active TSS	HUES64 Cell Line	embryonic stem cell
10	chr15:77924600-77927600	Enhancers	Fetal Heart	heart
11	chr15:77925600-77926800	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
12	chr15:77925800-77926600	Bivalent Enhancer	GM12878-XiMat	blood
13	chr15:77925800-77926800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr15:77925800-77926800	Bivalent Enhancer	Fetal Thymus	thymus
15	chr15:77925800-77927000	Bivalent Enhancer	Stomach Mucosa	stomach
16	chr15:77925800-77928000	Bivalent Enhancer	Fetal Brain Male	brain
17	chr15:77926000-77926600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr15:77926000-77926600	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr15:77926000-77926600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr15:77926000-77926600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
21	chr15:77926000-77926600	Bivalent Enhancer	Fetal Intestine Small	intestine
22	chr15:77926000-77926600	Enhancers	Left Ventricle	heart
23	chr15:77926000-77926600	Enhancers	Placenta Amnion	Placenta Amnion
24	chr15:77926000-77926600	Flanking Active TSS	A549	lung
25	chr15:77926000-77926600	Flanking Active TSS	K562	blood
26	chr15:77926000-77926800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr15:77926000-77926800	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
28	chr15:77926000-77927000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
29	chr15:77926000-77927000	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
30	chr15:77926000-77927000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
31	chr15:77926000-77927000	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
32	chr15:77926000-77927000	Bivalent Enhancer	Liver	Liver
33	chr15:77926000-77927000	Enhancers	Gastric	stomach
34	chr15:77926000-77927000	Enhancers	Pancreas	Pancrea
35	chr15:77926000-77927000	Enhancers	Right Ventricle	heart
36	chr15:77926000-77927200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr15:77926000-77927200	Bivalent Enhancer	Fetal Muscle Leg	muscle
38	chr15:77926000-77927200	Genic enhancers	Right Atrium	heart
39	chr15:77926000-77927400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
40	chr15:77926000-77927400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
41	chr15:77926000-77927400	Bivalent Enhancer	Fetal Stomach	stomach
42	chr15:77926000-77927400	Enhancers	Spleen	Spleen
43	chr15:77926000-77927600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
44	chr15:77926000-77927600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
45	chr15:77926000-77927600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
46	chr15:77926000-77927600	Bivalent Enhancer	Placenta	Placenta
47	chr15:77926200-77926600	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
48	chr15:77926200-77926600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr15:77926200-77926600	Bivalent Enhancer	Colon Smooth Muscle	Colon
50	chr15:77926200-77926600	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain

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