Variant report

Variant	esv1836749
Chromosome Location	chr15:77302969-77332606
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1215)
CpG islands
(count:854)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1215 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:77324454-77324600	HepG2	liver:	n/a	n/a
2	ATF2	chr15:77306145-77306892	GM12878	blood:	n/a	n/a
3	ATF2	chr15:77316619-77316962	GM12878	blood:	n/a	n/a
4	ATF2	chr15:77314226-77314800	GM12878	blood:	n/a	n/a
5	ATF2	chr15:77306056-77307216	GM12878	blood:	n/a	n/a
6	ATF2	chr15:77314306-77314560	GM12878	blood:	n/a	n/a
7	BACH1	chr15:77320425-77320611	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr15:77306056-77306497	GM12878	blood:	n/a	chr15:77306290-77306300 chr15:77306289-77306300 chr15:77306286-77306296
9	BATF	chr15:77306094-77306473	GM12878	blood:	n/a	chr15:77306290-77306300 chr15:77306289-77306300 chr15:77306286-77306296
10	BATF	chr15:77312280-77312501	GM12878	blood:	n/a	n/a
11	BCL11A	chr15:77306807-77307126	GM12878	blood:	n/a	n/a
12	BCL11A	chr15:77306811-77307122	GM12878	blood:	n/a	n/a
13	BCL3	chr15:77325266-77325980	A549	lung:	n/a	n/a
14	BCL3	chr15:77326777-77327284	A549	lung:	n/a	n/a
15	BCL3	chr15:77327427-77328043	A549	lung:	n/a	n/a
16	BCL3	chr15:77319746-77319961	GM12878	blood:	n/a	n/a
17	BCL3	chr15:77325651-77326184	A549	lung:	n/a	n/a
18	BCL3	chr15:77319696-77320041	GM12878	blood:	n/a	n/a
19	BCL3	chr15:77326463-77328028	A549	lung:	n/a	n/a
20	BCLAF1	chr15:77306496-77307260	GM12878	blood:	n/a	n/a
21	BHLHE40	chr15:77319232-77319473	HepG2	liver:	n/a	n/a
22	BHLHE40	chr15:77323768-77323927	GM12878	blood:	n/a	n/a
23	BHLHE40	chr15:77320463-77320709	K562	blood:	n/a	chr15:77320651-77320667
24	BHLHE40	chr15:77306097-77307171	GM12878	blood:	n/a	chr15:77306365-77306381
25	BHLHE40	chr15:77319308-77319431	K562	blood:	n/a	n/a
26	BHLHE40	chr15:77327273-77327720	K562	blood:	n/a	chr15:77327366-77327387 chr15:77327372-77327381 chr15:77327370-77327383 chr15:77327371-77327380 chr15:77327372-77327381
27	BHLHE40	chr15:77312372-77312424	GM12878	blood:	n/a	n/a
28	BHLHE40	chr15:77316652-77316796	K562	blood:	n/a	n/a
29	BHLHE40	chr15:77320006-77320083	K562	blood:	n/a	n/a
30	BHLHE40	chr15:77315646-77315869	K562	blood:	n/a	n/a
31	BRCA1	chr15:77316763-77316878	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr15:77306336-77306522	GM12878	blood:	n/a	n/a
33	CCNT2	chr15:77320595-77320914	K562	blood:	n/a	n/a
34	CEBPB	chr15:77306488-77306571	HepG2	liver:	n/a	n/a
35	CEBPB	chr15:77324292-77324502	HepG2	liver:	n/a	n/a
36	CEBPB	chr15:77312536-77312661	K562	blood:	n/a	chr15:77312579-77312590
37	CEBPB	chr15:77312427-77312735	HepG2	liver:	n/a	chr15:77312579-77312590
38	CEBPB	chr15:77330718-77330925	Hela-S3	cervix:	n/a	chr15:77330791-77330804
39	CEBPB	chr15:77316733-77316956	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr15:77312440-77312720	A549	lung:	n/a	chr15:77312579-77312590
41	CEBPB	chr15:77314436-77314701	IMR90	lung:	n/a	n/a
42	CEBPD	chr15:77324291-77324757	HepG2	liver:	n/a	n/a
43	CHD1	chr15:77311660-77311805	GM12878	blood:	n/a	n/a
44	CHD1	chr15:77306089-77307083	GM12878	blood:	n/a	n/a
45	CHD2	chr15:77327435-77327673	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr15:77327544-77327607	HepG2	liver:	n/a	n/a
47	CHD2	chr15:77316213-77316223	HepG2	liver:	n/a	n/a
48	CHD2	chr15:77329799-77329867	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr15:77316658-77316664	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr15:77320794-77320880	K562	blood:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:77320787-77320837	AG09309	skin:	n/a
2	chr15:77320787-77320837	Caco-2	colon:	n/a
3	chr15:77324751-77324801	ECC-1	luminal epithelium:	n/a
4	chr15:77320787-77320837	ovcar-3	ovarian:	n/a
5	chr15:77320211-77320261	AG09319	gingival:	n/a
6	chr15:77324751-77324801	HCF	heart:	n/a
7	chr15:77320384-77320434	LNCaP	prostate:	n/a
8	chr15:77327887-77327937	AG09319	gingival:	n/a
9	chr15:77324526-77324576	HRPEpiC	eye:	n/a
10	chr15:77324607-77324657	HAEpiC	amniotic membrane:	n/a
11	chr15:77324751-77324801	GM06990	blood:	n/a
12	chr15:77317370-77317420	U87	brain:	n/a
13	chr15:77323565-77323615	AG09309	skin:	n/a
14	chr15:77320787-77320837	NHDF-neo	bronchial:	n/a
15	chr15:77317370-77317420	NT2-D1	testis:	n/a
16	chr15:77324607-77324657	BJ	skin:	n/a
17	chr15:77314406-77314456	IMR90	lung:	fetal
18	chr15:77326735-77326785	H1-hESC	embryonic stem cell:	embryo
19	chr15:77317370-77317420	GM12891	blood:	n/a
20	chr15:77324607-77324657	HMEC	breast:	n/a
21	chr15:77320787-77320837	HCT-116	colon:	n/a
22	chr15:77320672-77320722	HepG2	liver:	n/a
23	chr15:77327887-77327937	IMR90	lung:	fetal
24	chr15:77314406-77314456	AG04449	skin:	fetal
25	chr15:77327887-77327937	NHBE	bronchial:	n/a
26	chr15:77324758-77324808	HepG2	liver:	n/a
27	chr15:77324751-77324801	LNCaP	prostate:	n/a
28	chr15:77323565-77323615	SK-N-SH_RA	brain:	n/a
29	chr15:77324526-77324576	HPAEpiC	pulmonary alveolar:	n/a
30	chr15:77320261-77320311	GM06990	blood:	n/a
31	chr15:77320672-77320722	HUVEC	blood vessel:	n/a
32	chr15:77324751-77324801	NB4	blood:	n/a
33	chr15:77320211-77320261	AoSMC	blood vessel:	n/a
34	chr15:77320672-77320722	GM12891	blood:	n/a
35	chr15:77323565-77323615	Jurkat	blood:	n/a
36	chr15:77320211-77320261	U87	brain:	n/a
37	chr15:77317370-77317420	HEK293	kidney:	embryo
38	chr15:77327887-77327937	T-47D	breast:	n/a
39	chr15:77324526-77324576	T-47D	breast:	n/a
40	chr15:77320384-77320434	ovcar-3	ovarian:	n/a
41	chr15:77320672-77320722	MCF-7	breast:	n/a
42	chr15:77320672-77320722	HCT-116	colon:	n/a
43	chr15:77324751-77324801	H1-hESC	embryonic stem cell:	embryo
44	chr15:77320384-77320434	HCF	heart:	n/a
45	chr15:77324607-77324657	HNPCEpiC	eye:	n/a
46	chr15:77324758-77324808	HL-60	blood:	n/a
47	chr15:77314406-77314456	HUVEC	blood vessel:	n/a
48	chr15:77320787-77320837	SKMC	muscle:	n/a
49	chr15:77320787-77320837	HCM	heart:	n/a
50	chr15:77320261-77320311	HCT-116	colon:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:77320466..77323005-chr15:77324460..77327682,3	MCF-7	breast:
2	chr15:77320639..77324428-chr15:77362244..77364696,3	K562	blood:
3	chr15:77325493..77328166-chr15:77329882..77331634,3	MCF-7	breast:
4	chr15:77316409..77317242-chr15:77835418..77836097,2	MCF-7	breast:
5	chr15:77315639..77319825-chr15:77322811..77328362,7	MCF-7	breast:
6	chr15:77316351..77317289-chr15:77788854..77789825,3	K562	blood:
7	chr15:77311951..77316312-chr15:77325010..77329080,4	K562	blood:
8	chr15:77316331..77317283-chr15:77835334..77836400,5	K562	blood:
9	chr15:77316379..77317255-chr15:77925626..77926458,2	MCF-7	breast:
10	chr15:77320466..77323005-chr15:77324460..77327682,3	MCF-7	breast:
11	chr15:77327656..77330194-chr15:77332164..77335172,3	K562	blood:
12	chr15:77316407..77317258-chr15:77399611..77400626,4	MCF-7	breast:
13	chr15:77327656..77329511-chr15:77332033..77335172,3	K562	blood:
14	chr15:77265440..77266266-chr15:77305789..77306421,2	MCF-7	breast:
15	chr15:77328280..77330879-chr15:77355103..77356921,2	K562	blood:
16	chr15:77316659..77317287-chr15:77410867..77411851,3	MCF-7	breast:
17	chr15:77303183..77305636-chr15:77307103..77311098,3	K562	blood:
18	chr15:77305426..77307546-chr15:77319169..77320927,2	K562	blood:
19	chr15:77265408..77266372-chr15:77316053..77316927,2	MCF-7	breast:
20	chr15:77332598..77335104-chr15:77338074..77339723,2	MCF-7	breast:

No data

Variant related genes	Relation type
PSTPIP1	TF binding region
ENSG00000259652	TF binding region
PSTPIP1	CpG island
ENSG00000259652	CpG island
ENSG00000140368	chromatin interactions
ENSG00000140391	chromatin interactions

Extended variants
information (count: 1489 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:1489 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11639459	chr15:77302969-77302970	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs542853723	chr15:77302992-77302993	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs115864060	chr15:77302995-77302996	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574074119	chr15:77303015-77303016	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544721948	chr15:77303020-77303021	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576945434	chr15:77303043-77303044	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs562828458	chr15:77303057-77303058	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs192817830	chr15:77303102-77303103	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs62027307	chr15:77303108-77303109	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs185334795	chr15:77303113-77303114	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs377712845	chr15:77303114-77303115	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370427607	chr15:77303116-77303117	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567173307	chr15:77303144-77303145	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535869161	chr15:77303159-77303160	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs7175783	chr15:77303265-77303266	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs187870253	chr15:77303272-77303273	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs569767739	chr15:77303279-77303280	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs538335440	chr15:77303311-77303312	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs567489599	chr15:77303356-77303357	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs558378599	chr15:77303373-77303374	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs578103911	chr15:77303412-77303413	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs538032246	chr15:77303428-77303429	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs534349577	chr15:77303480-77303481	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs150850150	chr15:77303482-77303483	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs571245169	chr15:77303483-77303484	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs554509883	chr15:77303507-77303508	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs538673788	chr15:77303557-77303558	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs553762507	chr15:77303584-77303585	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs74545169	chr15:77303598-77303599	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs370184738	chr15:77303626-77303627	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs139372275	chr15:77303640-77303641	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs554882846	chr15:77303664-77303665	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs62027308	chr15:77303692-77303693	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs543245476	chr15:77303693-77303694	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs556668291	chr15:77303710-77303711	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs8030698	chr15:77303739-77303740	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs192967258	chr15:77303740-77303741	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs560078872	chr15:77303746-77303747	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs527997972	chr15:77303748-77303749	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs542940166	chr15:77303755-77303756	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs561405744	chr15:77303787-77303788	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs531972361	chr15:77303842-77303843	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs556929070	chr15:77303853-77303854	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs562847523	chr15:77303876-77303877	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs2469207	chr15:77304000-77304001	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs576525828	chr15:77304036-77304037	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs571322405	chr15:77304062-77304063	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs532211613	chr15:77304114-77304115	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs184256158	chr15:77304147-77304148	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs547439197	chr15:77304148-77304149	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1130 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:77289200-77311200	Weak transcription	Aorta	Aorta
2	chr15:77289400-77305200	Weak transcription	Esophagus	oesophagus
3	chr15:77289400-77310000	Weak transcription	Colon Smooth Muscle	Colon
4	chr15:77290200-77306000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr15:77295600-77305200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
6	chr15:77295800-77305000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr15:77296200-77305000	Weak transcription	Thymus	Thymus
8	chr15:77296200-77305400	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr15:77296600-77306600	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr15:77299200-77304400	Genic enhancers	Primary neutrophils fromperipheralblood	blood
11	chr15:77299200-77304400	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
12	chr15:77299200-77304400	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
13	chr15:77299200-77305600	Genic enhancers	Primary monocytes fromperipheralblood	blood
14	chr15:77300400-77305000	Enhancers	Primary T killer memory cells from peripheral blood	blood
15	chr15:77301000-77305000	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr15:77301200-77304400	Genic enhancers	Monocytes-CD14+_RO01746	blood
17	chr15:77301200-77305000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr15:77301200-77305000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
19	chr15:77301400-77304400	Genic enhancers	Primary B cells from peripheral blood	blood
20	chr15:77301400-77304400	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
21	chr15:77301400-77305200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr15:77302000-77304000	Enhancers	Primary B cells from cord blood	blood
23	chr15:77302200-77303000	Enhancers	Pancreas	Pancrea
24	chr15:77302200-77303000	Genic enhancers	Spleen	Spleen
25	chr15:77302200-77303800	Enhancers	Fetal Thymus	thymus
26	chr15:77302200-77303800	Enhancers	GM12878-XiMat	blood
27	chr15:77302200-77304800	Weak transcription	Lung	lung
28	chr15:77302400-77303800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr15:77302400-77305400	Enhancers	Primary T helper cells fromperipheralblood	blood
30	chr15:77302600-77303400	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr15:77302600-77303400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr15:77302600-77303800	Enhancers	Primary hematopoietic stem cells	blood
33	chr15:77302800-77304000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr15:77302800-77304800	Weak transcription	Duodenum Mucosa	Duodenum
35	chr15:77302800-77305000	Enhancers	Primary T cells from cord blood	blood
36	chr15:77302800-77305200	Enhancers	Primary T cells fromperipheralblood	blood
37	chr15:77302800-77305800	Weak transcription	Adipose Nuclei	Adipose
38	chr15:77302800-77307600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr15:77303000-77307400	Enhancers	Spleen	Spleen
40	chr15:77303000-77319600	Weak transcription	Pancreas	Pancrea
41	chr15:77303400-77305000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
42	chr15:77303400-77305200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr15:77303800-77304000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr15:77303800-77304800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr15:77303800-77304800	Weak transcription	Fetal Thymus	thymus
46	chr15:77303800-77305000	Weak transcription	GM12878-XiMat	blood
47	chr15:77303800-77305200	Weak transcription	Primary hematopoietic stem cells	blood
48	chr15:77304000-77304400	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
49	chr15:77304000-77304600	Weak transcription	Primary B cells from cord blood	blood
50	chr15:77304400-77305000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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