Variant report

Variant	rs13329256
Chromosome Location	chr15:77926260-77926261
allele	A/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	TCF12	chr15:77926244-77926550	H1-hESC	embryonic stem cell:	n/a	n/a
2	TAF7	chr15:77925687-77926502	H1-hESC	embryonic stem cell:	n/a	n/a
3	ZBTB7A	chr15:77925228-77926263	ECC-1	luminal epithelium:	n/a	n/a
4	NANOG	chr15:77926237-77926527	H1-hESC	embryonic stem cell:	n/a	chr15:77926346-77926355
5	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
6	ZNF263	chr15:77923899-77927072	HEK293-T-REx	kidney:	n/a	chr15:77924758-77924767 chr15:77926052-77926061 chr15:77925322-77925331 chr15:77926338-77926347
7	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
8	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
9	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
10	ZNF263	chr15:77924464-77926639	K562	blood:	n/a	chr15:77924758-77924767 chr15:77926052-77926061 chr15:77925322-77925331 chr15:77926338-77926347
11	BACH1	chr15:77925619-77926520	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL3	chr15:77925412-77926262	A549	lung:	n/a	chr15:77925420-77925433
13	GTF2F1	chr15:77925850-77926594	H1-hESC	embryonic stem cell:	n/a	n/a
14	MXI1	chr15:77925637-77926993	H1-hESC	embryonic stem cell:	n/a	n/a
15	YY1	chr15:77925725-77927051	H1-hESC	embryonic stem cell:	n/a	chr15:77926548-77926559
16	MXI1	chr15:77925361-77926571	IMR90	lung:	n/a	n/a
17	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
18	E2F6	chr15:77925342-77926317	H1-hESC	embryonic stem cell:	n/a	n/a
19	MAZ	chr15:77925053-77926446	IMR90	lung:	n/a	chr15:77925671-77925678 chr15:77926409-77926419
20	MAX	chr15:77925367-77926267	ECC-1	luminal epithelium:	n/a	chr15:77925671-77925678
21	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
22	EP300	chr15:77925747-77926533	H1-hESC	embryonic stem cell:	n/a	n/a
23	TEAD4	chr15:77925695-77927069	H1-hESC	embryonic stem cell:	n/a	n/a
24	RAD21	chr15:77925660-77926391	HCT-116	colon:	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
25	SP1	chr15:77925672-77926289	A549	lung:	n/a	chr15:77925924-77925936 chr15:77925926-77925935
26	GABPA	chr15:77925734-77926420	H1-hESC	embryonic stem cell:	n/a	n/a
27	MAFK	chr15:77925836-77926293	Hela-S3	cervix:	n/a	n/a
28	ZNF143	chr15:77925145-77927535	H1-hESC	embryonic stem cell:	n/a	chr15:77925310-77925328 chr15:77927084-77927103 chr15:77927155-77927173 chr15:77926483-77926501
29	MAX	chr15:77925072-77926605	H1-hESC	embryonic stem cell:	n/a	chr15:77925671-77925678 chr15:77926530-77926539 chr15:77926409-77926419
30	YY1	chr15:77925714-77926482	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr15:77925542-77927058	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr15:77926220-77926370	AG04449	skin:	n/a	chr15:77926344-77926353
33	CTBP2	chr15:77925487-77927481	H1-hESC	embryonic stem cell:	n/a	n/a
34	TEAD4	chr15:77925733-77927104	H1-hESC	embryonic stem cell:	n/a	n/a
35	SIN3A	chr15:77925513-77927021	H1-hESC	embryonic stem cell:	n/a	chr15:77926561-77926569
36	POLR2A	chr15:77926242-77926444	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr15:77926257-77926315	Kidney_OC	kidney:	n/a	n/a
38	YY1	chr15:77925772-77926265	A549	lung:	n/a	n/a
39	JUND	chr15:77925811-77926924	H1-hESC	embryonic stem cell:	n/a	n/a
40	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
41	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
42	CTCF	chr15:77925666-77926278	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
43	RAD21	chr15:77925602-77926340	MCF-7	breast:	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
44	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
45	RAD21	chr15:77925762-77926260	ECC-1	luminal epithelium:	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
46	CREB1	chr15:77925792-77926741	H1-hESC	embryonic stem cell:	n/a	n/a
47	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
48	MAX	chr15:77925533-77926303	A549	lung:	n/a	chr15:77925671-77925678
49	CTCF	chr15:77926247-77926401	GM19240	blood:	n/a	chr15:77926344-77926353
50	CTCF	chr15:77926257-77926383	GM19239	blood:	n/a	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	chr15:77925249..77927257-chr15:78113205..78115049,24	MCF-7	breast:
5	chr15:77925299..77927652-chr15:78112444..78114100,3	MCF-7	breast:
6	chr15:77925435..77927439-chr15:78112259..78115090,22	K562	blood:
7	chr15:77835764..77836461-chr15:77925509..77926265,4	MCF-7	breast:
8	chr15:77925566..77926501-chr15:77951718..77952824,3	K562	blood:
9	chr15:77316379..77317255-chr15:77925626..77926458,2	MCF-7	breast:
10	chr15:77923251..77928296-chr15:78111448..78115771,8	MCF-7	breast:
11	chr15:77924601..77927275-chr15:77937272..77938910,2	K562	blood:
12	chr15:77925397..77928069-chr15:78112259..78116246,3	K562	blood:
13	chr15:77925519..77926294-chr15:78162494..78163468,3	MCF-7	breast:
14	chr15:77861324..77862294-chr15:77925777..77926357,2	K562	blood:
15	chr15:77925532..77926425-chr15:78076783..78078398,4	MCF-7	breast:
16	chr15:77925887..77926426-chr19:40734602..40735348,2	MCF-7	breast:
17	chr15:77925072..77927787-chr15:78111223..78115888,59	MCF-7	breast:
18	chr15:77909817..77910574-chr15:77925500..77926398,3	MCF-7	breast:
19	chr15:77925509..77926398-chr15:78076937..78077835,4	K562	blood:
20	chr15:77925492..77926460-chr15:77947054..77947731,3	K562	blood:
21	chr15:77925750..77926474-chr15:78007678..78008229,2	MCF-7	breast:
22	chr15:77838960..77839788-chr15:77925715..77926415,4	MCF-7	breast:
23	chr15:77835401..77836400-chr15:77925681..77926470,4	K562	blood:
24	chr15:77924941..77926828-chr15:77932359..77934227,2	MCF-7	breast:
25	chr15:77925397..77927315-chr15:78112259..78115116,2	K562	blood:
26	chr15:77925387..77926440-chr15:77951721..77952677,7	MCF-7	breast:
27	chr15:77478581..77479511-chr15:77925565..77926440,3	MCF-7	breast:
28	chr11:60252998..60253911-chr15:77925589..77926334,2	MCF-7	breast:
29	chr15:77925576..77926405-chr15:78167119..78167924,3	K562	blood:
30	chr15:77925580..77926309-chr15:78156358..78157211,2	MCF-7	breast:

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

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs11630768	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11633639	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11634778	0.83[CHB][hapmap];0.86[JPT][hapmap];0.86[ASN][1000 genomes]
rs11635239	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11638318	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11855155	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.98[LWK][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11856978	0.90[CHB][hapmap]
rs11857045	0.91[CHB][hapmap]
rs13329323	0.98[AFR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16969027	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1877292	0.86[JPT][hapmap]
rs1877294	0.83[CHB][hapmap];0.90[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]
rs2292415	0.85[CEU][hapmap];0.91[CHB][hapmap];0.93[JPT][hapmap];1.00[TSI][hapmap];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2292416	0.85[CEU][hapmap];0.91[CHB][hapmap];0.93[JPT][hapmap];1.00[TSI][hapmap];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2292417	0.85[CEU][hapmap];0.91[CHB][hapmap];0.93[JPT][hapmap];1.00[TSI][hapmap];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28374408	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28503184	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28515899	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56717248	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56941158	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs60886924	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7165679	0.83[CHB][hapmap];0.90[GIH][hapmap];0.81[JPT][hapmap]
rs7171716	0.91[CHB][hapmap];0.81[JPT][hapmap]
rs74025333	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74025334	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs74025342	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs74025352	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8024724	0.91[CHB][hapmap]
rs8024932	0.83[CHB][hapmap];0.85[GIH][hapmap]
rs8026164	0.83[CHB][hapmap];0.81[JPT][hapmap]
rs8026671	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8027456	0.91[CHB][hapmap]
rs8028788	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]
rs9652488	0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9806280	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9920101	0.83[CHB][hapmap];0.85[GIH][hapmap];0.81[JPT][hapmap]
rs9920113	0.91[CHB][hapmap]
rs9920127	0.83[CHB][hapmap];0.90[GIH][hapmap];0.81[JPT][hapmap]
rs9920132	0.89[GIH][hapmap];0.81[JPT][hapmap]
rs9920134	0.91[CHB][hapmap]
rs9920869	0.83[CHB][hapmap];0.80[JPT][hapmap]
rs9972481	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]

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:99 , 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	chr15:77923600-77926400	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	chr15:77924400-77926600	Active TSS	H1 Cell Line	embryonic stem cell
7	chr15:77924400-77926600	Active TSS	iPS-18 Cell Line	embryonic stem cell
8	chr15:77924600-77926600	Active TSS	iPS-20b Cell Line	embryonic stem cell
9	chr15:77924600-77927000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
10	chr15:77924600-77927400	Active TSS	HUES64 Cell Line	embryonic stem cell
11	chr15:77924600-77927600	Enhancers	Fetal Heart	heart
12	chr15:77924800-77926400	Active TSS	HUES6 Cell Line	embryonic stem cell
13	chr15:77925400-77926400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr15:77925400-77926400	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
15	chr15:77925400-77926400	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
16	chr15:77925600-77926400	Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr15:77925600-77926400	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
18	chr15:77925600-77926400	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
19	chr15:77925600-77926800	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
20	chr15:77925800-77926400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr15:77925800-77926400	Bivalent Enhancer	Fetal Lung	lung
22	chr15:77925800-77926600	Bivalent Enhancer	GM12878-XiMat	blood
23	chr15:77925800-77926800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr15:77925800-77926800	Bivalent Enhancer	Fetal Thymus	thymus
25	chr15:77925800-77927000	Bivalent Enhancer	Stomach Mucosa	stomach
26	chr15:77925800-77928000	Bivalent Enhancer	Fetal Brain Male	brain
27	chr15:77926000-77926400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr15:77926000-77926400	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr15:77926000-77926400	Flanking Active TSS	Brain Anterior Caudate	brain
30	chr15:77926000-77926400	Flanking Active TSS	Brain Cingulate Gyrus	brain
31	chr15:77926000-77926400	Flanking Active TSS	Brain Hippocampus Middle	brain
32	chr15:77926000-77926400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
33	chr15:77926000-77926400	Flanking Active TSS	Brain Substantia Nigra	brain
34	chr15:77926000-77926400	Flanking Active TSS	Hela-S3	cervix
35	chr15:77926000-77926400	Enhancers	NHDF-Ad	bronchial
36	chr15:77926000-77926400	Bivalent Enhancer	NHEK	skin
37	chr15:77926000-77926600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr15:77926000-77926600	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr15:77926000-77926600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr15:77926000-77926600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
41	chr15:77926000-77926600	Bivalent Enhancer	Fetal Intestine Small	intestine
42	chr15:77926000-77926600	Enhancers	Left Ventricle	heart
43	chr15:77926000-77926600	Enhancers	Placenta Amnion	Placenta Amnion
44	chr15:77926000-77926600	Flanking Active TSS	A549	lung
45	chr15:77926000-77926600	Flanking Active TSS	K562	blood
46	chr15:77926000-77926800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr15:77926000-77926800	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
48	chr15:77926000-77927000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
49	chr15:77926000-77927000	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
50	chr15:77926000-77927000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--

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