Variant report

Variant	esv2760033
Chromosome Location	chr15:56736478-56790080
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:878)
CpG islands
(count:854)
Chromatin interactive
region (count:20)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:878 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:56788756-56789177	K562	blood:	n/a	chr15:56788814-56788830
2	ARID3A	chr15:56757439-56757589	K562	blood:	n/a	n/a
3	ARID3A	chr15:56757183-56757342	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:56788752-56789118	HepG2	liver:	n/a	chr15:56788814-56788830
5	ATF1	chr15:56761692-56762037	K562	blood:	n/a	n/a
6	ATF1	chr15:56785297-56785306	K562	blood:	n/a	n/a
7	ATF2	chr15:56757025-56757555	GM12878	blood:	n/a	n/a
8	ATF3	chr15:56767569-56767875	K562	blood:	n/a	n/a
9	BACH1	chr15:56757137-56757703	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr15:56757918-56757978	K562	blood:	n/a	n/a
11	BATF	chr15:56788822-56789212	GM12878	blood:	n/a	n/a
12	BCL3	chr15:56757037-56757647	GM12878	blood:	n/a	n/a
13	BCL3	chr15:56757103-56757795	A549	lung:	n/a	n/a
14	BCLAF1	chr15:56757083-56757625	GM12878	blood:	n/a	n/a
15	BHLHE40	chr15:56757494-56757730	HepG2	liver:	n/a	n/a
16	BHLHE40	chr15:56783358-56783670	GM12878	blood:	n/a	n/a
17	BHLHE40	chr15:56757184-56757611	K562	blood:	n/a	chr15:56757254-56757270
18	CBX3	chr15:56757309-56757702	K562	blood:	n/a	n/a
19	CBX3	chr15:56757101-56757760	K562	blood:	n/a	n/a
20	CCNT2	chr15:56757151-56757524	K562	blood:	n/a	n/a
21	CEBPB	chr15:56752307-56752555	K562	blood:	n/a	n/a
22	CEBPB	chr15:56788802-56789166	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr15:56767591-56767871	A549	lung:	n/a	chr15:56767741-56767752
24	CEBPB	chr15:56788854-56789190	IMR90	lung:	n/a	n/a
25	CEBPB	chr15:56767644-56767889	Hela-S3	cervix:	n/a	chr15:56767741-56767752
26	CEBPB	chr15:56767576-56767913	K562	blood:	n/a	chr15:56767741-56767752
27	CEBPB	chr15:56748579-56748651	A549	lung:	n/a	n/a
28	CEBPB	chr15:56788774-56789197	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr15:56767650-56767857	H1-hESC	embryonic stem cell:	n/a	chr15:56767741-56767752
30	CEBPB	chr15:56767633-56767903	HepG2	liver:	n/a	chr15:56767741-56767752
31	CEBPB	chr15:56767580-56767912	IMR90	lung:	n/a	chr15:56767741-56767752
32	CEBPB	chr15:56788871-56789188	K562	blood:	n/a	n/a
33	CEBPB	chr15:56757311-56757566	K562	blood:	n/a	n/a
34	CHD1	chr15:56756836-56757173	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD1	chr15:56783168-56784219	IMR90	lung:	n/a	n/a
36	CHD2	chr15:56757084-56757599	GM12878	blood:	n/a	chr15:56757214-56757224
37	CHD2	chr15:56783380-56783542	GM12878	blood:	n/a	n/a
38	CHD2	chr15:56757151-56757631	K562	blood:	n/a	chr15:56757214-56757224
39	CHD2	chr15:56757109-56757659	H1-hESC	embryonic stem cell:	n/a	chr15:56757214-56757224
40	CHD2	chr15:56757172-56757543	HepG2	liver:	n/a	chr15:56757214-56757224
41	CREB1	chr15:56757090-56757700	A549	lung:	n/a	n/a
42	CTCF	chr15:56788812-56789210	MCF-7	breast:	n/a	chr15:56788921-56788942 chr15:56788919-56788937 chr15:56788920-56788936
43	CTCF	chr15:56783348-56783670	GM12878	blood:	n/a	chr15:56783511-56783532 chr15:56783514-56783522 chr15:56783509-56783527 chr15:56783510-56783526 chr15:56783512-56783525
44	CTCF	chr15:56788860-56789010	GM12866	blood:	n/a	chr15:56788921-56788942 chr15:56788919-56788937 chr15:56788920-56788936
45	CTCF	chr15:56788880-56789030	MCF-7	breast:	n/a	chr15:56788921-56788942 chr15:56788919-56788937 chr15:56788920-56788936
46	CTCF	chr15:56788817-56789077	Gliobla	brain:	n/a	chr15:56788921-56788942 chr15:56788919-56788937 chr15:56788920-56788936
47	CTCF	chr15:56757440-56757590	HEK293	kidney:	n/a	n/a
48	CTCF	chr15:56783760-56783910	GM12870	blood:	n/a	n/a
49	CTCF	chr15:56789220-56789370	HPF	lung:	n/a	n/a
50	CTCF	chr15:56788820-56788970	HUVEC	blood vessel:	n/a	chr15:56788921-56788942 chr15:56788919-56788937 chr15:56788920-56788936

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:56757180-56757230	NHBE	bronchial:	n/a
2	chr15:56757325-56757375	HCM	heart:	n/a
3	chr15:56757312-56757362	GM19239	blood:	n/a
4	chr15:56759655-56759705	SAEC	small airway:	n/a
5	chr15:56757806-56757856	BJ	skin:	n/a
6	chr15:56757382-56757432	GM12892	blood:	n/a
7	chr15:56758270-56758320	HCPEpiC	choroid plexus:	n/a
8	chr15:56757325-56757375	HAEpiC	amniotic membrane:	n/a
9	chr15:56757625-56757675	HUVEC	blood vessel:	n/a
10	chr15:56757108-56757158	T-47D	breast:	n/a
11	chr15:56757108-56757158	HMEC	breast:	n/a
12	chr15:56757180-56757230	NB4	blood:	n/a
13	chr15:56758270-56758320	PFSK-1	brain:	n/a
14	chr15:56757625-56757675	HIPEpiC	eye:	n/a
15	chr15:56759655-56759705	HEK293	kidney:	embryo
16	chr15:56757625-56757675	SK-N-SH_RA	brain:	n/a
17	chr15:56757625-56757675	NH-A	brain:	n/a
18	chr15:56757625-56757675	LNCaP	prostate:	n/a
19	chr15:56757108-56757158	GM12878	blood:	n/a
20	chr15:56757625-56757675	HPAEpiC	pulmonary alveolar:	n/a
21	chr15:56757290-56757340	SKMC	muscle:	n/a
22	chr15:56757312-56757362	HCT-116	colon:	n/a
23	chr15:56757382-56757432	Caco-2	colon:	n/a
24	chr15:56757312-56757362	HL-60	blood:	n/a
25	chr15:56758270-56758320	HAEpiC	amniotic membrane:	n/a
26	chr15:56759655-56759705	BJ	skin:	n/a
27	chr15:56757382-56757432	HL-60	blood:	n/a
28	chr15:56757180-56757230	HIPEpiC	eye:	n/a
29	chr15:56758270-56758320	LNCaP	prostate:	n/a
30	chr15:56757625-56757675	PANC-1	pancreas:	n/a
31	chr15:56757625-56757675	NB4	blood:	n/a
32	chr15:56757499-56757549	AG10803	skin:	n/a
33	chr15:56757382-56757432	HMEC	breast:	n/a
34	chr15:56757325-56757375	A549	lung:	n/a
35	chr15:56757382-56757432	HRE	kidney:	n/a
36	chr15:56757552-56757602	BE2_C	brain:	n/a
37	chr15:56757290-56757340	PANC-1	pancreas:	n/a
38	chr15:56757314-56757364	H1-hESC	embryonic stem cell:	embryo
39	chr15:56757499-56757549	GM19239	blood:	n/a
40	chr15:56757290-56757340	PrEC	prostate:	n/a
41	chr15:56757499-56757549	SK-N-MC	brain:	n/a
42	chr15:56757290-56757340	SAEC	small airway:	n/a
43	chr15:56757552-56757602	HIPEpiC	eye:	n/a
44	chr15:56757552-56757602	PANC-1	pancreas:	n/a
45	chr15:56757517-56757567	HMEC	breast:	n/a
46	chr15:56757806-56757856	IMR90	lung:	fetal
47	chr15:56757108-56757158	HL-60	blood:	n/a
48	chr15:56757806-56757856	U87	brain:	n/a
49	chr15:56757314-56757364	HRE	kidney:	n/a
50	chr15:56758270-56758320	Jurkat	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr15:56788851..56789408-chr15:57103635..57104349,2	MCF-7	breast:
2	chr15:56788753..56789362-chr15:57161247..57161954,2	K562	blood:
3	chr15:56762921..56765735-chr15:56765770..56767934,2	K562	blood:
4	chr15:56788863..56789371-chr16:34759996..34760825,2	MCF-7	breast:
5	chr15:56788688..56789403-chr15:57430424..57431057,2	MCF-7	breast:
6	chr15:56775436..56776246-chr15:56784313..56784975,2	K562	blood:
7	chr15:56783040..56784156-chr15:57161563..57162645,6	K562	blood:
8	chr15:56731142..56732969-chr15:56736651..56738760,2	K562	blood:
9	chr15:56773647..56776313-chr15:57177229..57179430,2	K562	blood:
10	chr15:56782685..56785505-chr15:57019755..57021681,2	K562	blood:
11	chr15:56788702..56789394-chr15:57161523..57162414,2	MCF-7	breast:
12	chr15:56782970..56783589-chr15:57598753..57599463,2	MCF-7	breast:
13	chr15:56756734..56759056-chr15:56761429..56763544,2	K562	blood:
14	chr15:56762921..56765735-chr15:56765770..56767934,2	K562	blood:
15	chr15:56788444..56789415-chr15:57598413..57599206,3	K562	blood:
16	chr15:56536083..56538918-chr15:56762516..56765231,2	K562	blood:
17	chr15:56537987..56538847-chr15:56756234..56756979,2	MCF-7	breast:
18	chr15:56775436..56776246-chr15:56784313..56784975,2	K562	blood:
19	chr15:56788456..56789162-chr15:57113822..57114589,2	MCF-7	breast:
20	chr15:56787707..56790107-chr15:57597582..57600140,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF280D-2	chr15:56755978-56756445	NONHSAT044023
2	lnc-ZNF280D-2	chr15:56757168-56757283	NONHSAT044023

No data

Variant related genes	Relation type
MNS1	TF binding region
MNS1	CpG island
ENSG00000151575	chromatin interactions
ENSG00000138587	chromatin interactions

Extended variants
information (count: 1995 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1995 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6493858	chr15:56736478-56736479	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs113855769	chr15:56736488-56736489	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs576538398	chr15:56736558-56736559	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs538960347	chr15:56736562-56736563	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs114511129	chr15:56736570-56736571	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs139192065	chr15:56736578-56736579	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs34616078	chr15:56736583-56736584	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs372539931	chr15:56736614-56736615	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532777553	chr15:56736625-56736626	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs369961031	chr15:56736630-56736631	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs144146491	chr15:56736671-56736672	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35775595	chr15:56736681-56736682	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs560540681	chr15:56736716-56736717	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs549395315	chr15:56736723-56736724	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs141270550	chr15:56736733-56736734	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574496323	chr15:56736744-56736745	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs16976912	chr15:56736767-56736768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375847167	chr15:56736768-56736769	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201457984	chr15:56736779-56736780	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs369951910	chr15:56736785-56736786	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs139643304	chr15:56736790-56736791	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532301407	chr15:56736796-56736797	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs144284822	chr15:56736840-56736841	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs369837125	chr15:56736848-56736849	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111534825	chr15:56736860-56736861	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs367708963	chr15:56736863-56736864	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs146561870	chr15:56736867-56736868	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189338493	chr15:56736878-56736879	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528384773	chr15:56736881-56736882	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375664797	chr15:56736882-56736883	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372819169	chr15:56736889-56736890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181873152	chr15:56736892-56736893	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567603216	chr15:56736902-56736903	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs377218859	chr15:56736912-56736913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs60405436	chr15:56736922-56736923	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs371938307	chr15:56736925-56736926	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs144803743	chr15:56736965-56736966	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs570175126	chr15:56737043-56737044	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538872423	chr15:56737095-56737096	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs113349371	chr15:56737123-56737124	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs185273027	chr15:56737151-56737152	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534986198	chr15:56737239-56737240	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs528972310	chr15:56737248-56737249	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190216389	chr15:56737260-56737261	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs73415841	chr15:56737285-56737286	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs7170307	chr15:56737297-56737298	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs568714902	chr15:56737306-56737307	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563369788	chr15:56737335-56737336	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576991095	chr15:56737349-56737350	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs554856304	chr15:56737517-56737518	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	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
Colorectal cancer	16774939	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
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Gastric adenocarcinoma	19115996	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:698 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:56690000-56737800	Weak transcription	Stomach Mucosa	stomach
2	chr15:56716000-56756600	Weak transcription	HSMM	muscle
3	chr15:56718600-56736600	Weak transcription	Brain Hippocampus Middle	brain
4	chr15:56718600-56756200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr15:56719200-56742400	Weak transcription	Fetal Intestine Large	intestine
6	chr15:56719400-56736800	Weak transcription	Fetal Muscle Leg	muscle
7	chr15:56720800-56740600	Weak transcription	GM12878-XiMat	blood
8	chr15:56721400-56737600	Weak transcription	Pancreas	Pancrea
9	chr15:56721800-56736600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr15:56722400-56736800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr15:56722800-56746800	Weak transcription	Thymus	Thymus
12	chr15:56723400-56756600	Weak transcription	Fetal Stomach	stomach
13	chr15:56723600-56737400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr15:56731000-56738600	Strong transcription	Dnd41	blood
15	chr15:56732200-56756800	Weak transcription	Fetal Brain Male	brain
16	chr15:56732800-56742000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr15:56733000-56739800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr15:56734600-56736800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr15:56734800-56751200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr15:56735000-56738200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr15:56735000-56738400	Strong transcription	Fetal Lung	lung
22	chr15:56735000-56739600	Weak transcription	Fetal Muscle Trunk	muscle
23	chr15:56735000-56739800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr15:56735200-56740200	Weak transcription	Osteobl	bone
25	chr15:56735200-56756400	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr15:56735400-56736800	Weak transcription	Ovary	ovary
27	chr15:56735400-56739800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr15:56735400-56756600	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr15:56735600-56737400	Weak transcription	Primary hematopoietic stem cells	blood
30	chr15:56735600-56756400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr15:56735600-56756600	Weak transcription	Brain Anterior Caudate	brain
32	chr15:56736000-56751200	Weak transcription	Fetal Thymus	thymus
33	chr15:56736200-56736800	Strong transcription	Fetal Kidney	kidney
34	chr15:56736400-56755200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr15:56736800-56738000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr15:56736800-56754400	Weak transcription	Fetal Kidney	kidney
37	chr15:56737800-56738200	Enhancers	Stomach Mucosa	stomach
38	chr15:56738000-56739600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr15:56738400-56756200	Weak transcription	Fetal Lung	lung
40	chr15:56738600-56743400	Weak transcription	Dnd41	blood
41	chr15:56739600-56756600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr15:56743200-56756800	Weak transcription	Aorta	Aorta
43	chr15:56743400-56744600	Strong transcription	Dnd41	blood
44	chr15:56744200-56744400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr15:56744400-56744600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr15:56744600-56751600	Weak transcription	Dnd41	blood
47	chr15:56744600-56757200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr15:56746800-56747800	Enhancers	HUVEC	blood vessel
49	chr15:56747000-56747200	Enhancers	Stomach Mucosa	stomach
50	chr15:56747000-56747400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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