Variant report

Variant	esv3359172
Chromosome Location	chr15:41856320-41857334
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:108)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:108 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:41856735-41856820	HepG2	liver:	n/a	n/a
2	BHLHE40	chr15:41856582-41856875	K562	blood:	n/a	n/a
3	CBX3	chr15:41856619-41857025	K562	blood:	n/a	n/a
4	CCNT2	chr15:41857032-41857519	K562	blood:	n/a	n/a
5	CHD2	chr15:41856278-41856935	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD2	chr15:41857158-41857210	HepG2	liver:	n/a	n/a
7	CHD2	chr15:41856521-41856926	HepG2	liver:	n/a	n/a
8	CHD2	chr15:41856693-41856931	K562	blood:	n/a	n/a
9	CTCF	chr15:41856840-41856990	HepG2	liver:	n/a	n/a
10	CTCF	chr15:41856480-41856630	HCPEpiC	choroid plexus:	n/a	n/a
11	CTCF	chr15:41856480-41856630	HRE	kidney:	n/a	n/a
12	CTCF	chr15:41856516-41856590	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr15:41856520-41856670	BE2_C	brain:	n/a	n/a
14	CTCF	chr15:41856480-41856630	HPAF	blood vessel:	n/a	n/a
15	CTCF	chr15:41856480-41856630	SK-N-SH_RA	brain:	n/a	n/a
16	CTCF	chr15:41856460-41856610	AG04450	lung:	n/a	n/a
17	CTCF	chr15:41856480-41856630	K562	blood:	n/a	n/a
18	CTCF	chr15:41856440-41856590	HPAF	blood vessel:	n/a	n/a
19	CTCF	chr15:41856460-41856610	HPF	lung:	n/a	n/a
20	CTCF	chr15:41856500-41856650	SK-N-SH_RA	brain:	n/a	n/a
21	CTCF	chr15:41856400-41856550	BE2_C	brain:	n/a	n/a
22	CTCF	chr15:41856640-41856790	BE2_C	brain:	n/a	n/a
23	CTCF	chr15:41856880-41857030	BE2_C	brain:	n/a	n/a
24	CTCF	chr15:41856500-41856650	HepG2	liver:	n/a	n/a
25	CTCF	chr15:41856500-41856650	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr15:41856460-41856610	HEK293	kidney:	n/a	n/a
27	EGR1	chr15:41856703-41856938	K562	blood:	n/a	chr15:41856788-41856801
28	ELF1	chr15:41857274-41857556	K562	blood:	n/a	n/a
29	ELK1	chr15:41856856-41856948	K562	blood:	n/a	n/a
30	EP300	chr15:41856675-41856934	K562	blood:	n/a	n/a
31	EP300	chr15:41856532-41856873	H1-hESC	embryonic stem cell:	n/a	n/a
32	EP300	chr15:41856731-41856960	SK-N-SH_RA	brain:	n/a	n/a
33	FOXA1	chr15:41856628-41856960	HepG2	liver:	n/a	n/a
34	FOXP2	chr15:41856640-41856982	PFSK-1	brain:	n/a	n/a
35	FOXP2	chr15:41856641-41856971	PFSK-1	brain:	n/a	n/a
36	GTF2F1	chr15:41856598-41856918	H1-hESC	embryonic stem cell:	n/a	n/a
37	GTF2F1	chr15:41856556-41856597	K562	blood:	n/a	n/a
38	HDAC2	chr15:41856486-41856941	HepG2	liver:	n/a	n/a
39	JUND	chr15:41856602-41856824	K562	blood:	n/a	chr15:41856666-41856675
40	JUND	chr15:41856659-41856917	H1-hESC	embryonic stem cell:	n/a	chr15:41856666-41856675
41	MAFK	chr15:41857013-41857137	HepG2	liver:	n/a	n/a
42	MAX	chr15:41856631-41857013	K562	blood:	n/a	n/a
43	MAX	chr15:41857301-41857385	K562	blood:	n/a	n/a
44	MAX	chr15:41857143-41857561	K562	blood:	n/a	n/a
45	MAZ	chr15:41857319-41857553	K562	blood:	n/a	n/a
46	MAZ	chr15:41856513-41857022	K562	blood:	n/a	n/a
47	MAZ	chr15:41856380-41857080	IMR90	lung:	n/a	n/a
48	MAZ	chr15:41856674-41856742	Hela-S3	cervix:	n/a	n/a
49	MAZ	chr15:41856600-41856946	HepG2	liver:	n/a	n/a
50	MYC	chr15:41856798-41856924	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:41856520-41856570	SK-N-MC	brain:	n/a
2	chr15:41856520-41856570	NB4	blood:	n/a
3	chr15:41856520-41856570	HAEpiC	amniotic membrane:	n/a
4	chr15:41856520-41856570	GM12892	blood:	n/a
5	chr15:41856520-41856570	BE2_C	brain:	n/a
6	chr15:41856520-41856570	HCM	heart:	n/a
7	chr15:41856520-41856570	HCPEpiC	choroid plexus:	n/a
8	chr15:41856520-41856570	NHDF-neo	bronchial:	n/a
9	chr15:41856520-41856570	HepG2	liver:	n/a
10	chr15:41856520-41856570	AG04450	lung:	fetal
11	chr15:41856520-41856570	PANC-1	pancreas:	n/a
12	chr15:41856520-41856570	HCF	heart:	n/a
13	chr15:41856520-41856570	AG10803	skin:	n/a
14	chr15:41856520-41856570	SAEC	small airway:	n/a
15	chr15:41856520-41856570	H1-hESC	embryonic stem cell:	embryo
16	chr15:41856520-41856570	HCT-116	colon:	n/a
17	chr15:41856520-41856570	K562	blood:	n/a
18	chr15:41856520-41856570	HUVEC	blood vessel:	n/a
19	chr15:41856520-41856570	HL-60	blood:	n/a
20	chr15:41856520-41856570	HPAEpiC	pulmonary alveolar:	n/a
21	chr15:41856520-41856570	SK-N-SH_RA	brain:	n/a
22	chr15:41856520-41856570	HMEC	breast:	n/a
23	chr15:41856520-41856570	HRE	kidney:	n/a
24	chr15:41856520-41856570	PrEC	prostate:	n/a
25	chr15:41856520-41856570	Hela-S3	cervix:	n/a
26	chr15:41856520-41856570	LNCaP	prostate:	n/a
27	chr15:41856520-41856570	AG04449	skin:	fetal
28	chr15:41856520-41856570	Caco-2	colon:	n/a
29	chr15:41856520-41856570	GM19239	blood:	n/a
30	chr15:41856520-41856570	T-47D	breast:	n/a
31	chr15:41856520-41856570	MCF-7	breast:	n/a
32	chr15:41856520-41856570	GM12891	blood:	n/a
33	chr15:41856520-41856570	IMR90	lung:	fetal
34	chr15:41856520-41856570	SK-N-SH	brain:	n/a
35	chr15:41856520-41856570	MCF10A-Er-Src	breast:	n/a
36	chr15:41856520-41856570	HIPEpiC	eye:	n/a
37	chr15:41856520-41856570	BJ	skin:	n/a
38	chr15:41856520-41856570	HEK293	kidney:	embryo
39	chr15:41856520-41856570	RPTEC	kidney:	n/a
40	chr15:41856520-41856570	HRPEpiC	eye:	n/a
41	chr15:41856520-41856570	AG09309	skin:	n/a
42	chr15:41856520-41856570	HRCEpiC	kidney:	n/a
43	chr15:41856520-41856570	Hepatocyte	liver:	n/a
44	chr15:41856520-41856570	Jurkat	blood:	n/a
45	chr15:41856520-41856570	AoSMC	blood vessel:	n/a
46	chr15:41856520-41856570	HEEpiC	esophagus:	n/a
47	chr15:41856520-41856570	ProgFib	skin:	n/a
48	chr15:41856520-41856570	NH-A	brain:	n/a
49	chr15:41856520-41856570	GM12878	blood:	n/a
50	chr15:41856520-41856570	GM06990	blood:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:41853373..41858542-chr15:41950830..41955637,10	K562	blood:
2	chr15:41854411..41856736-chr15:42132704..42135389,2	K562	blood:
3	chr15:41849459..41853162-chr15:41854225..41857161,4	MCF-7	breast:
4	chr15:41856836..41858542-chr15:41952173..41953837,2	K562	blood:
5	chr15:41853749..41856717-chr15:41950905..41954753,5	K562	blood:

No data

Variant related genes	Relation type
TYRO3	TF binding region
TYRO3	CpG island
ENSG00000243708	chromatin interactions
ENSG00000174197	chromatin interactions
ENSG00000092445	chromatin interactions

Extended variants
information (count: 42 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:42 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376621156	chr15:41856337-41856338	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs117224665	chr15:41856350-41856351	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs201165681	chr15:41856376-41856377	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs375507876	chr15:41856400-41856401	Enhancers Flanking Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs138227584	chr15:41856401-41856402	Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs369311519	chr15:41856417-41856418	Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs76520897	chr15:41856424-41856425	Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs199792732	chr15:41856443-41856444	Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs557270589	chr15:41856456-41856457	Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs373641420	chr15:41856520-41856521	Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs573845570	chr15:41856533-41856534	Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs2289742	chr15:41856541-41856542	Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs11070339	chr15:41856543-41856544	Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs572480863	chr15:41856563-41856564	Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs537220234	chr15:41856576-41856577	Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs544721085	chr15:41856692-41856693	Flanking Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs564614409	chr15:41856723-41856724	Flanking Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs558785782	chr15:41856746-41856747	Flanking Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs575839089	chr15:41856790-41856791	Flanking Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs141684866	chr15:41856856-41856857	Flanking Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs561490671	chr15:41856915-41856916	Flanking Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs530330376	chr15:41856956-41856957	Flanking Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs137899210	chr15:41856962-41856963	Flanking Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs115828781	chr15:41856987-41856988	Flanking Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs532534832	chr15:41857019-41857020	Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs552733745	chr15:41857058-41857059	Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs569370994	chr15:41857062-41857063	Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs2277537	chr15:41857080-41857081	Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs367744324	chr15:41857108-41857109	Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs567409850	chr15:41857115-41857116	Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs536179816	chr15:41857126-41857127	Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs552816337	chr15:41857131-41857132	Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs74715543	chr15:41857137-41857138	Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs11639399	chr15:41857216-41857217	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs199551494	chr15:41857219-41857220	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs201774612	chr15:41857252-41857253	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs141776232	chr15:41857258-41857259	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs376761841	chr15:41857276-41857277	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs150579508	chr15:41857277-41857278	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs2277536	chr15:41857303-41857304	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs141641556	chr15:41857307-41857308	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs373160779	chr15:41857321-41857322	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelofibrosis	22110671	CNVD
Maculopathy	20981449	CNVD
Gastric adenocarcinoma	19115996	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:130 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:41852200-41877400	Weak transcription	Aorta	Aorta
2	chr15:41852400-41859600	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr15:41852400-41860600	Weak transcription	HUVEC	blood vessel
4	chr15:41852400-41877200	Weak transcription	Colon Smooth Muscle	Colon
5	chr15:41852600-41856800	Enhancers	HepG2	liver
6	chr15:41852600-41858600	Weak transcription	NHDF-Ad	bronchial
7	chr15:41852600-41859600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr15:41852600-41877400	Weak transcription	HMEC	breast
9	chr15:41852800-41857600	Genic enhancers	Fetal Stomach	stomach
10	chr15:41852800-41877400	Weak transcription	NHEK	skin
11	chr15:41853000-41856400	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr15:41853000-41856400	Weak transcription	Lung	lung
13	chr15:41853000-41861800	Genic enhancers	Fetal Intestine Large	intestine
14	chr15:41853000-41862000	Genic enhancers	Fetal Intestine Small	intestine
15	chr15:41853200-41858200	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr15:41853200-41860200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr15:41853200-41861800	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr15:41853200-41863200	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr15:41853200-41872600	Weak transcription	Hela-S3	cervix
20	chr15:41853400-41856600	Weak transcription	Right Ventricle	heart
21	chr15:41853400-41857400	Enhancers	Ovary	ovary
22	chr15:41853400-41859400	Genic enhancers	HUES64 Cell Line	embryonic stem cell
23	chr15:41853400-41859800	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr15:41853400-41870600	Weak transcription	Stomach Mucosa	stomach
25	chr15:41853600-41857200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr15:41853600-41857600	Genic enhancers	HUES48 Cell Line	embryonic stem cell
27	chr15:41853600-41859800	Genic enhancers	H1 Cell Line	embryonic stem cell
28	chr15:41853600-41860000	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr15:41853600-41862200	Weak transcription	Duodenum Mucosa	Duodenum
30	chr15:41853800-41856400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
31	chr15:41853800-41861400	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
32	chr15:41853800-41864000	Genic enhancers	Brain Cingulate Gyrus	brain
33	chr15:41854000-41860200	Strong transcription	Dnd41	blood
34	chr15:41854000-41860800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr15:41854000-41871400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr15:41854200-41856600	Enhancers	H9 Cell Line	embryonic stem cell
37	chr15:41854200-41857800	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr15:41854200-41859600	Weak transcription	Pancreas	Pancrea
39	chr15:41854200-41877000	Weak transcription	Fetal Brain Male	brain
40	chr15:41854400-41857000	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr15:41854400-41857600	Strong transcription	Fetal Brain Female	brain
42	chr15:41854600-41856400	Genic enhancers	HUES6 Cell Line	embryonic stem cell
43	chr15:41854600-41856400	Genic enhancers	Brain Substantia Nigra	brain
44	chr15:41854600-41857200	Enhancers	Fetal Thymus	thymus
45	chr15:41854800-41857000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr15:41854800-41857400	Genic enhancers	Fetal Muscle Leg	muscle
47	chr15:41855000-41857400	Genic enhancers	Fetal Lung	lung
48	chr15:41855000-41858200	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr15:41855000-41861400	Genic enhancers	Brain Anterior Caudate	brain
50	chr15:41855200-41857400	Enhancers	Spleen	Spleen

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