Variant report

Variant	esv3312256
Chromosome Location	chr15:41854897-41856388
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:109)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:109 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:41855096-41855276	K562	blood:	n/a	n/a
2	BCL3	chr15:41854865-41855368	K562	blood:	n/a	n/a
3	BHLHE40	chr15:41854934-41855528	K562	blood:	n/a	n/a
4	CBX3	chr15:41854889-41855496	K562	blood:	n/a	n/a
5	CHD2	chr15:41855044-41855345	K562	blood:	n/a	n/a
6	CHD2	chr15:41856278-41856935	H1-hESC	embryonic stem cell:	n/a	n/a
7	CUX1	chr15:41855210-41855354	K562	blood:	n/a	n/a
8	EGR1	chr15:41854894-41855478	K562	blood:	n/a	chr15:41855256-41855269
9	EGR1	chr15:41855011-41855429	K562	blood:	n/a	chr15:41855256-41855269
10	ELF1	chr15:41854912-41855412	K562	blood:	n/a	n/a
11	EP300	chr15:41855002-41855416	K562	blood:	n/a	chr15:41855086-41855102
12	ETS1	chr15:41854972-41855252	K562	blood:	n/a	n/a
13	ETS1	chr15:41854920-41855408	K562	blood:	n/a	n/a
14	GABPA	chr15:41854924-41855446	K562	blood:	n/a	n/a
15	GABPA	chr15:41854871-41855357	K562	blood:	n/a	n/a
16	GATA2	chr15:41854901-41855432	K562	blood:	n/a	chr15:41855097-41855110
17	HCFC1	chr15:41855158-41855250	K562	blood:	n/a	n/a
18	HDAC2	chr15:41854935-41855433	K562	blood:	n/a	n/a
19	HDAC2	chr15:41854893-41855392	K562	blood:	n/a	n/a
20	JUND	chr15:41855055-41855418	K562	blood:	n/a	n/a
21	MAFK	chr15:41854925-41855256	K562	blood:	n/a	n/a
22	MAX	chr15:41855065-41855272	K562	blood:	n/a	n/a
23	MAX	chr15:41854988-41855384	K562	blood:	n/a	n/a
24	MAX	chr15:41854912-41855504	K562	blood:	n/a	n/a
25	MAZ	chr15:41854967-41855594	K562	blood:	n/a	n/a
26	MAZ	chr15:41856380-41857080	IMR90	lung:	n/a	n/a
27	MXI1	chr15:41855107-41855252	K562	blood:	n/a	n/a
28	MYC	chr15:41855025-41855571	K562	blood:	n/a	n/a
29	MYC	chr15:41855067-41855392	K562	blood:	n/a	n/a
30	NFIC	chr15:41856347-41856889	ECC-1	luminal epithelium:	n/a	n/a
31	NR2F2	chr15:41854782-41855510	K562	blood:	n/a	n/a
32	NR2F2	chr15:41854939-41855329	K562	blood:	n/a	n/a
33	PML	chr15:41854893-41855384	K562	blood:	n/a	n/a
34	PML	chr15:41854961-41855384	K562	blood:	n/a	n/a
35	POLR2A	chr15:41856213-41856924	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr15:41855360-41855420	Hela-S3	cervix:	n/a	n/a
37	POLR2A	chr15:41855180-41855527	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr15:41854875-41855709	K562	blood:	n/a	n/a
39	POLR2A	chr15:41855538-41855544	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr15:41856338-41857405	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr15:41856343-41856352	K562	blood:	n/a	n/a
42	POLR2A	chr15:41855433-41855461	K562	blood:	n/a	n/a
43	POLR2A	chr15:41856154-41856968	K562	blood:	n/a	n/a
44	POLR2A	chr15:41854944-41854966	HepG2	liver:	n/a	n/a
45	POLR2A	chr15:41854869-41855524	K562	blood:	n/a	n/a
46	POLR2A	chr15:41855023-41857639	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr15:41855236-41855463	K562	blood:	n/a	n/a
48	POLR2A	chr15:41854866-41856211	K562	blood:	n/a	n/a
49	POLR2A	chr15:41856229-41857524	K562	blood:	n/a	n/a
50	POLR2A	chr15:41853242-41855924	K562	blood:	n/a	n/a

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:41849971..41852250-chr15:41853838..41856239,2	MCF-7	breast:
2	chr15:41854411..41856736-chr15:42132704..42135389,2	K562	blood:
3	chr15:41853749..41856717-chr15:41950905..41954753,5	K562	blood:
4	chr15:41849459..41853162-chr15:41854225..41857161,4	MCF-7	breast:
5	chr15:41853373..41858542-chr15:41950830..41955637,10	K562	blood:
6	chr15:41853319..41856101-chr15:41857506..41859513,2	MCF-7	breast:
7	chr15:41853024..41855719-chr15:41894877..41896959,2	K562	blood:

No data

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

Extended variants
information (count: 56 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:56 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372252105	chr15:41854910-41854911	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs372293809	chr15:41854931-41854932	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs573908040	chr15:41854936-41854937	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs375283686	chr15:41854952-41854953	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs200261540	chr15:41854956-41854957	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs553174598	chr15:41855004-41855005	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs150490291	chr15:41855005-41855006	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs541222915	chr15:41855011-41855012	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs11636422	chr15:41855014-41855015	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs370921432	chr15:41855043-41855044	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs564191573	chr15:41855122-41855123	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs149181636	chr15:41855134-41855135	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs563316797	chr15:41855168-41855169	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs146593885	chr15:41855171-41855172	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs58793214	chr15:41855212-41855213	Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs528849725	chr15:41855222-41855223	Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs542742168	chr15:41855226-41855227	Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs181341627	chr15:41855278-41855279	Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs528709003	chr15:41855285-41855286	Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs186415094	chr15:41855322-41855323	Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs72739700	chr15:41855403-41855404	Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs543104041	chr15:41855418-41855419	Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs531116904	chr15:41855492-41855493	Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs561253270	chr15:41855493-41855494	Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs77455271	chr15:41855501-41855502	Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs190520311	chr15:41855522-41855523	Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs567684077	chr15:41855587-41855588	Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs536227558	chr15:41855662-41855663	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs372622476	chr15:41855684-41855685	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs1023194	chr15:41855729-41855730	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs1023193	chr15:41855736-41855737	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs539093409	chr15:41855776-41855777	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs557985947	chr15:41855777-41855778	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs7174076	chr15:41855846-41855847	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
35	rs577884198	chr15:41855868-41855869	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
36	rs543715739	chr15:41855873-41855874	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
37	rs1200339	chr15:41855932-41855933	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
38	rs573610577	chr15:41855933-41855934	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
39	rs182749182	chr15:41855934-41855935	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
40	rs145112875	chr15:41855939-41855940	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
41	rs186438128	chr15:41855958-41855959	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
42	rs3784285	chr15:41856003-41856004	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs368050263	chr15:41856028-41856029	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs565161087	chr15:41856059-41856060	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs190799430	chr15:41856098-41856099	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs551282595	chr15:41856105-41856106	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs567857448	chr15:41856109-41856110	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs530146761	chr15:41856136-41856137	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs371548867	chr15:41856166-41856167	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs546685534	chr15:41856167-41856168	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 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:151 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:41852200-41877400	Weak transcription	Aorta	Aorta
2	chr15:41852400-41855200	Weak transcription	HSMM	muscle
3	chr15:41852400-41859600	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr15:41852400-41860600	Weak transcription	HUVEC	blood vessel
5	chr15:41852400-41877200	Weak transcription	Colon Smooth Muscle	Colon
6	chr15:41852600-41855000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr15:41852600-41855000	Enhancers	Fetal Lung	lung
8	chr15:41852600-41855400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr15:41852600-41855400	Enhancers	Duodenum Smooth Muscle	Duodenum
10	chr15:41852600-41856800	Enhancers	HepG2	liver
11	chr15:41852600-41858600	Weak transcription	NHDF-Ad	bronchial
12	chr15:41852600-41859600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr15:41852600-41877400	Weak transcription	HMEC	breast
14	chr15:41852800-41855400	Enhancers	Fetal Muscle Trunk	muscle
15	chr15:41852800-41857600	Genic enhancers	Fetal Stomach	stomach
16	chr15:41852800-41877400	Weak transcription	NHEK	skin
17	chr15:41853000-41856000	Weak transcription	Fetal Heart	heart
18	chr15:41853000-41856400	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr15:41853000-41856400	Weak transcription	Lung	lung
20	chr15:41853000-41861800	Genic enhancers	Fetal Intestine Large	intestine
21	chr15:41853000-41862000	Genic enhancers	Fetal Intestine Small	intestine
22	chr15:41853200-41855600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr15:41853200-41858200	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr15:41853200-41860200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr15:41853200-41861800	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr15:41853200-41863200	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr15:41853200-41872600	Weak transcription	Hela-S3	cervix
28	chr15:41853400-41856600	Weak transcription	Right Ventricle	heart
29	chr15:41853400-41857400	Enhancers	Ovary	ovary
30	chr15:41853400-41859400	Genic enhancers	HUES64 Cell Line	embryonic stem cell
31	chr15:41853400-41859800	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr15:41853400-41870600	Weak transcription	Stomach Mucosa	stomach
33	chr15:41853600-41855000	Genic enhancers	Brain Angular Gyrus	brain
34	chr15:41853600-41855400	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr15:41853600-41855600	Enhancers	NH-A	brain
36	chr15:41853600-41856000	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr15:41853600-41856000	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr15:41853600-41856200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr15:41853600-41857200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr15:41853600-41857600	Genic enhancers	HUES48 Cell Line	embryonic stem cell
41	chr15:41853600-41859800	Genic enhancers	H1 Cell Line	embryonic stem cell
42	chr15:41853600-41860000	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr15:41853600-41862200	Weak transcription	Duodenum Mucosa	Duodenum
44	chr15:41853800-41855600	Transcr. at gene 5' and 3'	iPS-20b Cell Line	embryonic stem cell
45	chr15:41853800-41855600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr15:41853800-41856000	Genic enhancers	K562	blood
47	chr15:41853800-41856400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
48	chr15:41853800-41861400	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
49	chr15:41853800-41864000	Genic enhancers	Brain Cingulate Gyrus	brain
50	chr15:41854000-41855000	Enhancers	Brain Anterior Caudate	brain

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