Variant report

Variant	esv3351542
Chromosome Location	chr15:77223247-77225445
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:462)
CpG islands
(count:610)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:462 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:77223635-77223886	K562	blood:	n/a	n/a
2	ARID3A	chr15:77223253-77223963	HepG2	liver:	n/a	n/a
3	ATF1	chr15:77223343-77224161	K562	blood:	n/a	n/a
4	BACH1	chr15:77223488-77223541	K562	blood:	n/a	n/a
5	BCLAF1	chr15:77223480-77224429	GM12878	blood:	n/a	chr15:77223886-77223899 chr15:77224371-77224384 chr15:77224401-77224414
6	BHLHE40	chr15:77223610-77224281	K562	blood:	n/a	chr15:77223925-77223941
7	BHLHE40	chr15:77224473-77225324	GM12878	blood:	n/a	chr15:77225063-77225076 chr15:77225065-77225074 chr15:77225065-77225074 chr15:77225059-77225080 chr15:77225066-77225075
8	BHLHE40	chr15:77224491-77225243	K562	blood:	n/a	chr15:77225063-77225076 chr15:77225065-77225074 chr15:77225065-77225074 chr15:77225059-77225080 chr15:77225066-77225075
9	BHLHE40	chr15:77224631-77225130	HepG2	liver:	n/a	chr15:77225063-77225076 chr15:77225065-77225074 chr15:77225065-77225074 chr15:77225059-77225080 chr15:77225066-77225075
10	BRCA1	chr15:77223455-77224158	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr15:77223262-77224167	K562	blood:	n/a	n/a
12	CCNT2	chr15:77223729-77224493	K562	blood:	n/a	chr15:77223761-77223770
13	CEBPB	chr15:77223696-77224249	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr15:77223030-77223308	HepG2	liver:	n/a	chr15:77223143-77223156 chr15:77223144-77223155
15	CEBPB	chr15:77223005-77223369	Hela-S3	cervix:	n/a	chr15:77223143-77223156 chr15:77223144-77223155
16	CEBPB	chr15:77222999-77223388	K562	blood:	n/a	chr15:77223143-77223156 chr15:77223144-77223155
17	CEBPD	chr15:77223676-77224303	HepG2	liver:	n/a	n/a
18	CHD1	chr15:77224519-77225198	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr15:77223678-77224176	GM12878	blood:	n/a	chr15:77223891-77223901
20	CHD2	chr15:77223845-77224211	HepG2	liver:	n/a	chr15:77223891-77223901
21	CHD2	chr15:77223575-77224163	K562	blood:	n/a	chr15:77223891-77223901
22	CHD2	chr15:77223652-77224651	Hela-S3	cervix:	n/a	chr15:77223891-77223901
23	CHD2	chr15:77223781-77224246	H1-hESC	embryonic stem cell:	n/a	chr15:77223891-77223901
24	CREB1	chr15:77223763-77224175	A549	lung:	n/a	n/a
25	CREB1	chr15:77223670-77224313	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr15:77223678-77224311	GM12878	blood:	n/a	n/a
27	CREB1	chr15:77223526-77224394	HepG2	liver:	n/a	n/a
28	CREB1	chr15:77223688-77224340	K562	blood:	n/a	n/a
29	CREB1	chr15:77223646-77224439	A549	lung:	n/a	n/a
30	CTCF	chr15:77223640-77223790	HEK293	kidney:	n/a	n/a
31	CTCF	chr15:77224140-77224290	GM12873	blood:	n/a	n/a
32	CTCF	chr15:77223990-77224042	Pancreas_OC	pancreas:	n/a	n/a
33	CTCF	chr15:77224189-77224314	Lung_OC	lung:	n/a	n/a
34	CTCF	chr15:77223620-77223770	AG04449	skin:	n/a	n/a
35	CTCF	chr15:77223620-77223770	AG10803	skin:	n/a	n/a
36	CTCF	chr15:77224139-77224179	Lung_OC	lung:	n/a	n/a
37	CTCF	chr15:77224340-77224490	GM12866	blood:	n/a	n/a
38	CTCF	chr15:77224120-77224270	GM12869	blood:	n/a	n/a
39	CTCF	chr15:77224200-77224350	GM12871	blood:	n/a	n/a
40	CTCF	chr15:77223886-77224134	Lung_OC	lung:	n/a	n/a
41	CTCF	chr15:77224268-77224332	MCF-7	breast:	n/a	n/a
42	CTCF	chr15:77223800-77223950	GM12866	blood:	n/a	n/a
43	CTCF	chr15:77224195-77224280	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr15:77224235-77224326	MCF-7	breast:	n/a	n/a
45	CTCF	chr15:77223640-77223790	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr15:77224017-77224250	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr15:77224180-77224330	GM12874	blood:	n/a	n/a
48	CTCF	chr15:77224281-77224286	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr15:77224200-77224350	NHEK	skin:	n/a	n/a
50	CTCF	chr15:77223920-77224070	AG04449	skin:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:77224230-77224280	H1-hESC	embryonic stem cell:	embryo
2	chr15:77223867-77223917	HRPEpiC	eye:	n/a
3	chr15:77224587-77224637	AG10803	skin:	n/a
4	chr15:77223807-77223857	HAEpiC	amniotic membrane:	n/a
5	chr15:77223542-77223592	U87	brain:	n/a
6	chr15:77223542-77223592	AG04449	skin:	fetal
7	chr15:77223867-77223917	AG04449	skin:	fetal
8	chr15:77223719-77223769	HRE	kidney:	n/a
9	chr15:77224357-77224407	GM12892	blood:	n/a
10	chr15:77223980-77224030	HEK293	kidney:	embryo
11	chr15:77224357-77224407	IMR90	lung:	fetal
12	chr15:77224364-77224414	PFSK-1	brain:	n/a
13	chr15:77224364-77224414	PrEC	prostate:	n/a
14	chr15:77224230-77224280	HCT-116	colon:	n/a
15	chr15:77223807-77223857	ovcar-3	ovarian:	n/a
16	chr15:77224357-77224407	AG09309	skin:	n/a
17	chr15:77224587-77224637	H1-hESC	embryonic stem cell:	embryo
18	chr15:77223867-77223917	K562	blood:	n/a
19	chr15:77223867-77223917	HNPCEpiC	eye:	n/a
20	chr15:77223867-77223917	PANC-1	pancreas:	n/a
21	chr15:77223719-77223769	A549	lung:	n/a
22	chr15:77223867-77223917	IMR90	lung:	fetal
23	chr15:77223719-77223769	NT2-D1	testis:	n/a
24	chr15:77224230-77224280	HNPCEpiC	eye:	n/a
25	chr15:77224587-77224637	SK-N-MC	brain:	n/a
26	chr15:77224230-77224280	BE2_C	brain:	n/a
27	chr15:77224230-77224280	MCF10A-Er-Src	breast:	n/a
28	chr15:77223542-77223592	BE2_C	brain:	n/a
29	chr15:77223807-77223857	K562	blood:	n/a
30	chr15:77224364-77224414	HCF	heart:	n/a
31	chr15:77224230-77224280	BJ	skin:	n/a
32	chr15:77223867-77223917	SK-N-SH_RA	brain:	n/a
33	chr15:77223867-77223917	H1-hESC	embryonic stem cell:	embryo
34	chr15:77223867-77223917	HIPEpiC	eye:	n/a
35	chr15:77223719-77223769	ECC-1	luminal epithelium:	n/a
36	chr15:77224987-77225037	Hepatocyte	liver:	n/a
37	chr15:77224587-77224637	NB4	blood:	n/a
38	chr15:77224364-77224414	HNPCEpiC	eye:	n/a
39	chr15:77223980-77224030	AG04449	skin:	fetal
40	chr15:77223980-77224030	NT2-D1	testis:	n/a
41	chr15:77223980-77224030	AG09319	gingival:	n/a
42	chr15:77223719-77223769	Caco-2	colon:	n/a
43	chr15:77224364-77224414	HRPEpiC	eye:	n/a
44	chr15:77223867-77223917	CMK	blood:	n/a
45	chr15:77224587-77224637	GM19239	blood:	n/a
46	chr15:77224364-77224414	A549	lung:	n/a
47	chr15:77224357-77224407	HAEpiC	amniotic membrane:	n/a
48	chr15:77223807-77223857	HCF	heart:	n/a
49	chr15:77223980-77224030	IMR90	lung:	fetal
50	chr15:77223542-77223592	NB4	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:77195051..77197848-chr15:77221697..77224553,2	MCF-7	breast:
2	chr15:76584744..76587703-chr15:77223601..77225703,2	K562	blood:
3	chr15:77224456..77225977-chr15:77322256..77324914,2	K562	blood:
4	chr15:77223331..77224220-chr6:31795445..31796173,2	NB4	blood:
5	chr15:77213948..77217003-chr15:77220696..77223782,5	K562	blood:
6	chr15:77223524..77226032-chr15:77234679..77237040,2	MCF-7	breast:
7	chr15:77224127..77226874-chr15:77232246..77234714,2	K562	blood:
8	chr15:77208994..77210693-chr15:77221866..77223836,2	MCF-7	breast:
9	chr15:77196182..77198169-chr15:77222869..77226186,3	K562	blood:
10	chr15:77209000..77210645-chr15:77221529..77223671,2	K562	blood:
11	chr15:77194744..77199863-chr15:77220881..77225601,7	MCF-7	breast:
12	chr12:120729471..120731046-chr15:77223645..77226365,2	MCF-7	breast:
13	chr15:77196272..77198559-chr15:77223364..77225357,2	K562	blood:
14	chr15:77222222..77225627-chr15:77232795..77236028,3	K562	blood:

No data

Variant related genes	Relation type
RCN2	TF binding region
RCN2	CpG island
ENSG00000202538	chromatin interactions
ENSG00000117906	chromatin interactions
ENSG00000204388	chromatin interactions
ENSG00000140386	chromatin interactions
ENSG00000200795	chromatin interactions
ENSG00000140374	chromatin interactions
ENSG00000140368	chromatin interactions

Extended variants
information (count: 89 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:89 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3829489	chr15:77223256-77223257	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs557711238	chr15:77223381-77223382	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs117984138	chr15:77223392-77223393	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs79440396	chr15:77223396-77223397	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs555679903	chr15:77223401-77223402	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs185735095	chr15:77223413-77223414	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs190642989	chr15:77223428-77223429	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs147709411	chr15:77223434-77223435	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs530987655	chr15:77223452-77223453	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs536794102	chr15:77223460-77223461	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs375350176	chr15:77223470-77223471	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs557010469	chr15:77223497-77223498	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs372668231	chr15:77223564-77223565	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs149173950	chr15:77223590-77223591	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs543837523	chr15:77223593-77223594	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs564471278	chr15:77223638-77223639	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs528451989	chr15:77223682-77223683	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs546915303	chr15:77223684-77223685	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs528382691	chr15:77223703-77223704	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs367950197	chr15:77223716-77223717	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs3764244	chr15:77223740-77223741	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs59858088	chr15:77223755-77223756	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs150283820	chr15:77223771-77223772	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs568884044	chr15:77223772-77223773	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs539488191	chr15:77223786-77223787	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs71447131	chr15:77223828-77223829	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs398043523	chr15:77223832-77223833	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs557553748	chr15:77223846-77223847	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs181495237	chr15:77223869-77223870	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs533768181	chr15:77223936-77223937	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs555740558	chr15:77223968-77223969	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs573942694	chr15:77223972-77223973	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs537648395	chr15:77223985-77223986	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs556294689	chr15:77224008-77224009	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs374769638	chr15:77224017-77224018	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs546312014	chr15:77224019-77224020	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs564400916	chr15:77224022-77224023	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs572946866	chr15:77224023-77224024	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs540221073	chr15:77224026-77224027	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs533126822	chr15:77224108-77224109	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs529495010	chr15:77224110-77224111	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs550912225	chr15:77224145-77224146	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs1567672	chr15:77224242-77224243	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs563134720	chr15:77224261-77224262	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs533344320	chr15:77224321-77224322	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs551503219	chr15:77224378-77224379	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs566565044	chr15:77224402-77224403	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs551931641	chr15:77224406-77224407	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs533780439	chr15:77224420-77224421	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs548953798	chr15:77224449-77224450	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:501 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:77221200-77223400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr15:77221600-77223600	Weak transcription	Left Ventricle	heart
3	chr15:77222200-77223400	Enhancers	Fetal Intestine Small	intestine
4	chr15:77222400-77223400	Enhancers	Fetal Intestine Large	intestine
5	chr15:77223000-77223400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr15:77223000-77223400	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr15:77223000-77223400	Enhancers	Primary B cells from peripheral blood	blood
8	chr15:77223000-77223400	Enhancers	Primary T cells fromperipheralblood	blood
9	chr15:77223000-77223400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr15:77223000-77223400	Enhancers	Primary T helper naive cells from peripheral blood	blood
11	chr15:77223000-77223400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
12	chr15:77223000-77223400	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr15:77223000-77223400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
14	chr15:77223000-77223400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr15:77223000-77223400	Enhancers	Aorta	Aorta
16	chr15:77223000-77223400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr15:77223000-77223600	Flanking Active TSS	A549	lung
18	chr15:77223000-77223600	Flanking Active TSS	K562	blood
19	chr15:77223000-77223800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr15:77223000-77223800	Flanking Active TSS	Hela-S3	cervix
21	chr15:77223200-77223400	Enhancers	H1 Cell Line	embryonic stem cell
22	chr15:77223200-77223400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr15:77223200-77223400	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr15:77223200-77223400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
25	chr15:77223200-77223400	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr15:77223200-77223400	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr15:77223200-77223400	Active TSS	Primary B cells from cord blood	blood
28	chr15:77223200-77223400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr15:77223200-77223400	Enhancers	Primary T killer memory cells from peripheral blood	blood
30	chr15:77223200-77223400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr15:77223200-77223400	Enhancers	Muscle Satellite Cultured Cells	--
32	chr15:77223200-77223400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr15:77223200-77223400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr15:77223200-77223400	Enhancers	Adipose Nuclei	Adipose
35	chr15:77223200-77223400	Enhancers	Liver	Liver
36	chr15:77223200-77223400	Enhancers	Brain Angular Gyrus	brain
37	chr15:77223200-77223400	Enhancers	Colon Smooth Muscle	Colon
38	chr15:77223200-77223400	Active TSS	Fetal Brain Male	brain
39	chr15:77223200-77223400	Enhancers	Fetal Heart	heart
40	chr15:77223200-77223400	Enhancers	Fetal Kidney	kidney
41	chr15:77223200-77223400	Enhancers	Pancreatic Islets	Pancreatic Islet
42	chr15:77223200-77223400	Enhancers	Fetal Stomach	stomach
43	chr15:77223200-77223400	Active TSS	Skeletal Muscle Female	skeletal muscle
44	chr15:77223200-77223400	Enhancers	Stomach Mucosa	stomach
45	chr15:77223200-77223400	Enhancers	HMEC	breast
46	chr15:77223200-77223400	Active TSS	HUVEC	blood vessel
47	chr15:77223200-77223600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
48	chr15:77223200-77223600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
49	chr15:77223200-77223600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
50	chr15:77223200-77223600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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