Variant report

Variant	rs74025333
Chromosome Location	chr15:77926103-77926104
allele	C/T
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	MAX	chr15:77925511-77926168	Hela-S3	cervix:	n/a	chr15:77925671-77925678
2	MYBL2	chr15:77925748-77926221	HepG2	liver:	n/a	n/a
3	TAF7	chr15:77925687-77926502	H1-hESC	embryonic stem cell:	n/a	n/a
4	RAD21	chr15:77925787-77926186	A549	lung:	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
5	POLR2A	chr15:77925671-77926183	HCT-116	colon:	n/a	n/a
6	POLR2A	chr15:77925129-77926145	PFSK-1	brain:	n/a	n/a
7	HDAC2	chr15:77925793-77926130	K562	blood:	n/a	n/a
8	POLR2A	chr15:77925358-77926122	H1-hESC	embryonic stem cell:	n/a	n/a
9	MAX	chr15:77925474-77926231	HepG2	liver:	n/a	chr15:77925671-77925678
10	SIN3AK20	chr15:77925782-77926119	A549	lung:	n/a	n/a
11	CTCF	chr15:77925795-77926173	Fibrobl	skin:	n/a	chr15:77926005-77926023 chr15:77925949-77925962 chr15:77925947-77925963 chr15:77926008-77926021 chr15:77925946-77925964 chr15:77925948-77925969 chr15:77926007-77926028
12	MAX	chr15:77925474-77926117	SK-N-SH	brain:	n/a	chr15:77925671-77925678
13	ZBTB7A	chr15:77925228-77926263	ECC-1	luminal epithelium:	n/a	n/a
14	MAX	chr15:77925029-77926147	K562	blood:	n/a	chr15:77925671-77925678
15	CTCF	chr15:77925801-77926170	MCF-7	breast:	n/a	chr15:77926005-77926023 chr15:77925949-77925962 chr15:77925947-77925963 chr15:77926008-77926021 chr15:77925946-77925964 chr15:77925948-77925969 chr15:77926007-77926028
16	CTCF	chr15:77925799-77926165	K562	blood:	n/a	chr15:77926005-77926023 chr15:77925949-77925962 chr15:77925947-77925963 chr15:77926008-77926021 chr15:77925946-77925964 chr15:77925948-77925969 chr15:77926007-77926028
17	YY1	chr15:77925767-77926156	GM12878	blood:	n/a	n/a
18	SMC3	chr15:77925583-77926214	K562	blood:	n/a	chr15:77925870-77925880 chr15:77925948-77925962 chr15:77925912-77925922 chr15:77926007-77926021
19	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
20	ZNF263	chr15:77923899-77927072	HEK293-T-REx	kidney:	n/a	chr15:77924758-77924767 chr15:77926052-77926061 chr15:77925322-77925331 chr15:77926338-77926347
21	POLR2A	chr15:77925160-77926258	SK-N-MC	brain:	n/a	n/a
22	RAD21	chr15:77925823-77926154	GM12878	blood:	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
23	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
24	CTCF	chr15:77925556-77926199	GM12891	blood:	n/a	chr15:77926005-77926023 chr15:77925949-77925962 chr15:77925947-77925963 chr15:77926008-77926021 chr15:77925946-77925964 chr15:77925948-77925969 chr15:77926007-77926028
25	CTCF	chr15:77925797-77926177	Gliobla	brain:	n/a	chr15:77926005-77926023 chr15:77925949-77925962 chr15:77925947-77925963 chr15:77926008-77926021 chr15:77925946-77925964 chr15:77925948-77925969 chr15:77926007-77926028
26	CTCF	chr15:77925960-77926110	HAc	cerebellar:	n/a	chr15:77926005-77926023 chr15:77926008-77926021 chr15:77926007-77926028
27	CTCF	chr15:77925418-77926460	MCF-7	breast:	n/a	chr15:77926005-77926023 chr15:77925949-77925962 chr15:77925947-77925963 chr15:77926008-77926021 chr15:77925946-77925964 chr15:77925948-77925969 chr15:77926007-77926028 chr15:77926344-77926353
28	CTCF	chr15:77925573-77926424	GM19238	blood:	n/a	chr15:77926005-77926023 chr15:77925949-77925962 chr15:77925947-77925963 chr15:77926008-77926021 chr15:77925946-77925964 chr15:77925948-77925969 chr15:77926007-77926028 chr15:77926344-77926353
29	ZNF263	chr15:77924464-77926639	K562	blood:	n/a	chr15:77924758-77924767 chr15:77926052-77926061 chr15:77925322-77925331 chr15:77926338-77926347
30	MTA3	chr15:77925546-77926216	GM12878	blood:	n/a	n/a
31	BACH1	chr15:77925619-77926520	H1-hESC	embryonic stem cell:	n/a	n/a
32	BCL3	chr15:77925412-77926262	A549	lung:	n/a	chr15:77925420-77925433
33	CTCF	chr15:77925801-77926152	GM10248	blood:	n/a	chr15:77926005-77926023 chr15:77925949-77925962 chr15:77925947-77925963 chr15:77926008-77926021 chr15:77925946-77925964 chr15:77925948-77925969 chr15:77926007-77926028
34	POLR2A	chr15:77925843-77926155	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr15:77925796-77926155	Pancreas_OC	pancreas:	n/a	chr15:77926005-77926023 chr15:77925949-77925962 chr15:77925947-77925963 chr15:77926008-77926021 chr15:77925946-77925964 chr15:77925948-77925969 chr15:77926007-77926028
36	STAT1	chr15:77925891-77926118	GM12878	blood:	n/a	n/a
37	GTF2F1	chr15:77925850-77926594	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr15:77925671-77926253	HepG2	liver:	n/a	chr15:77926005-77926023 chr15:77925949-77925962 chr15:77925947-77925963 chr15:77926008-77926021 chr15:77925946-77925964 chr15:77925948-77925969 chr15:77926007-77926028
39	RAD21	chr15:77925777-77926168	SK-N-SH_RA	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
40	CTCF	chr15:77925697-77926153	ECC-1	luminal epithelium:	n/a	chr15:77926005-77926023 chr15:77925949-77925962 chr15:77925947-77925963 chr15:77926008-77926021 chr15:77925946-77925964 chr15:77925948-77925969 chr15:77926007-77926028
41	STAT5A	chr15:77925802-77926147	GM12878	blood:	n/a	n/a
42	CTCF	chr15:77925960-77926110	HCM	heart:	n/a	chr15:77926005-77926023 chr15:77926008-77926021 chr15:77926007-77926028
43	MXI1	chr15:77925637-77926993	H1-hESC	embryonic stem cell:	n/a	n/a
44	YY1	chr15:77925725-77927051	H1-hESC	embryonic stem cell:	n/a	chr15:77926548-77926559
45	CTCF	chr15:77925798-77926159	LNCaP	prostate:	n/a	chr15:77926005-77926023 chr15:77925949-77925962 chr15:77925947-77925963 chr15:77926008-77926021 chr15:77925946-77925964 chr15:77925948-77925969 chr15:77926007-77926028
46	MXI1	chr15:77925361-77926571	IMR90	lung:	n/a	n/a
47	CHD1	chr15:77925898-77926113	GM12878	blood:	n/a	n/a
48	TCF12	chr15:77925470-77926193	ECC-1	luminal epithelium:	n/a	chr15:77926169-77926179 chr15:77925956-77925966
49	MAX	chr15:77925431-77926105	SK-N-SH	brain:	n/a	chr15:77925671-77925678
50	CTCF	chr15:77925376-77926506	HCT-116	colon:	n/a	chr15:77926005-77926023 chr15:77925949-77925962 chr15:77925947-77925963 chr15:77926008-77926021 chr15:77925946-77925964 chr15:77925948-77925969 chr15:77926007-77926028 chr15:77926344-77926353

No.	Distal block	Cell Line	Cell type
1	chr15:77909277..77910127-chr15:77925790..77926339,2	MCF-7	breast:
2	chr15:77912184..77913186-chr15:77925455..77926450,5	K562	blood:
3	chr15:77925536..77926440-chr15:77946558..77947953,8	MCF-7	breast:
4	chr15:77925603..77926173-chr15:77946987..77947667,2	MCF-7	breast:
5	chr15:77925249..77927257-chr15:78113205..78115049,24	MCF-7	breast:
6	chr15:77925299..77927652-chr15:78112444..78114100,3	MCF-7	breast:
7	chr15:77925435..77927439-chr15:78112259..78115090,22	K562	blood:
8	chr15:77835764..77836461-chr15:77925509..77926265,4	MCF-7	breast:
9	chr15:77925566..77926501-chr15:77951718..77952824,3	K562	blood:
10	chr15:77316379..77317255-chr15:77925626..77926458,2	MCF-7	breast:
11	chr15:77923251..77928296-chr15:78111448..78115771,8	MCF-7	breast:
12	chr15:77924601..77927275-chr15:77937272..77938910,2	K562	blood:
13	chr15:77925397..77928069-chr15:78112259..78116246,3	K562	blood:
14	chr15:77925519..77926294-chr15:78162494..78163468,3	MCF-7	breast:
15	chr15:77478486..77479274-chr15:77925458..77926114,2	MCF-7	breast:
16	chr15:77861324..77862294-chr15:77925777..77926357,2	K562	blood:
17	chr15:77925532..77926425-chr15:78076783..78078398,4	MCF-7	breast:
18	chr15:77925887..77926426-chr19:40734602..40735348,2	MCF-7	breast:
19	chr15:77925072..77927787-chr15:78111223..78115888,59	MCF-7	breast:
20	chr15:77909817..77910574-chr15:77925500..77926398,3	MCF-7	breast:
21	chr15:77925509..77926398-chr15:78076937..78077835,4	K562	blood:
22	chr15:77925492..77926460-chr15:77947054..77947731,3	K562	blood:
23	chr15:77925750..77926474-chr15:78007678..78008229,2	MCF-7	breast:
24	chr15:77838960..77839788-chr15:77925715..77926415,4	MCF-7	breast:
25	chr15:77835401..77836400-chr15:77925681..77926470,4	K562	blood:
26	chr15:77924941..77926828-chr15:77932359..77934227,2	MCF-7	breast:
27	chr15:77925397..77927315-chr15:78112259..78115116,2	K562	blood:
28	chr15:77925387..77926440-chr15:77951721..77952677,7	MCF-7	breast:
29	chr15:77478581..77479511-chr15:77925565..77926440,3	MCF-7	breast:
30	chr11:60252998..60253911-chr15:77925589..77926334,2	MCF-7	breast:
31	chr15:77925576..77926405-chr15:78167119..78167924,3	K562	blood:
32	chr15:77925580..77926309-chr15:78156358..78157211,2	MCF-7	breast:

Variant related genes	Relation type
LINGO1	TF binding region
ENSG00000259666	Chromatin interaction
ENSG00000169783	Chromatin interaction
ENSG00000259281	Chromatin interaction

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs11630768	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11633639	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11634778	0.86[ASN][1000 genomes]
rs11635239	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11638318	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11852680	0.84[AFR][1000 genomes]
rs11854903	0.88[AFR][1000 genomes]
rs11855155	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13329256	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13329323	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16969027	0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1877298	0.88[AFR][1000 genomes]
rs1995972	0.88[AFR][1000 genomes]
rs2292415	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2292416	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2292417	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28374408	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28503184	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28515899	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28649029	0.86[AFR][1000 genomes]
rs28684542	0.84[AFR][1000 genomes]
rs56717248	0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56941158	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs60886924	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs74025334	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs74025342	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs74025352	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8026671	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8027963	0.84[AFR][1000 genomes]
rs8028788	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9652488	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9806280	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9920132	0.84[AFR][1000 genomes]
rs9972481	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 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	esv3327337	chr15:77923947-77926345	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
11	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:106 , 50 per page) page: 1 2 3

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	chr15:77923600-77926400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
4	chr15:77923600-77926600	Active TSS	iPS-15b Cell Line	embryonic stem cell
5	chr15:77924000-77927600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr15:77924400-77926200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr15:77924400-77926200	Active TSS	Brain Angular Gyrus	brain
8	chr15:77924400-77926600	Active TSS	H1 Cell Line	embryonic stem cell
9	chr15:77924400-77926600	Active TSS	iPS-18 Cell Line	embryonic stem cell
10	chr15:77924600-77926600	Active TSS	iPS-20b Cell Line	embryonic stem cell
11	chr15:77924600-77927000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
12	chr15:77924600-77927400	Active TSS	HUES64 Cell Line	embryonic stem cell
13	chr15:77924600-77927600	Enhancers	Fetal Heart	heart
14	chr15:77924800-77926400	Active TSS	HUES6 Cell Line	embryonic stem cell
15	chr15:77925200-77926200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr15:77925200-77926200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr15:77925200-77926200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr15:77925200-77926200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr15:77925400-77926200	Flanking Bivalent TSS/Enh	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr15:77925400-77926200	Flanking Bivalent TSS/Enh	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr15:77925400-77926200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr15:77925400-77926200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr15:77925400-77926200	Flanking Active TSS	Adipose Nuclei	Adipose
24	chr15:77925400-77926200	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
25	chr15:77925400-77926200	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
26	chr15:77925400-77926200	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
27	chr15:77925400-77926200	Flanking Bivalent TSS/Enh	NH-A	brain
28	chr15:77925400-77926400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr15:77925400-77926400	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
30	chr15:77925400-77926400	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
31	chr15:77925600-77926200	Bivalent/Poised TSS	Primary T cells from cord blood	blood
32	chr15:77925600-77926400	Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr15:77925600-77926400	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
34	chr15:77925600-77926400	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
35	chr15:77925600-77926800	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
36	chr15:77925800-77926200	Flanking Bivalent TSS/Enh	Primary B cells from cord blood	blood
37	chr15:77925800-77926200	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
38	chr15:77925800-77926200	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
39	chr15:77925800-77926200	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
40	chr15:77925800-77926200	Flanking Active TSS	HMEC	breast
41	chr15:77925800-77926200	Bivalent Enhancer	NHLF	lung
42	chr15:77925800-77926400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr15:77925800-77926400	Bivalent Enhancer	Fetal Lung	lung
44	chr15:77925800-77926600	Bivalent Enhancer	GM12878-XiMat	blood
45	chr15:77925800-77926800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr15:77925800-77926800	Bivalent Enhancer	Fetal Thymus	thymus
47	chr15:77925800-77927000	Bivalent Enhancer	Stomach Mucosa	stomach
48	chr15:77925800-77928000	Bivalent Enhancer	Fetal Brain Male	brain
49	chr15:77926000-77926200	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
50	chr15:77926000-77926200	Flanking Bivalent TSS/Enh	Primary B cells from peripheral blood	blood

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