Variant report

Variant	nsv1040028
Chromosome Location	chr15:43893072-43992646
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr15:43937873-43938217	GM12878	blood:	n/a	n/a
2	ATF2	chr15:43930649-43931067	GM12878	blood:	n/a	n/a
3	ATF2	chr15:43937824-43938301	GM12878	blood:	n/a	n/a
4	BATF	chr15:43931144-43931498	GM12878	blood:	n/a	n/a
5	BATF	chr15:43930739-43931096	GM12878	blood:	n/a	n/a
6	BATF	chr15:43931124-43931473	GM12878	blood:	n/a	n/a
7	BATF	chr15:43982183-43982550	GM12878	blood:	n/a	n/a
8	BATF	chr15:43937914-43938101	GM12878	blood:	n/a	n/a
9	BATF	chr15:43937842-43938114	GM12878	blood:	n/a	n/a
10	BCL11A	chr15:43938810-43938992	GM12878	blood:	n/a	n/a
11	BCL11A	chr15:43930706-43930979	GM12878	blood:	n/a	n/a
12	BCL11A	chr15:43930652-43931058	GM12878	blood:	n/a	chr15:43930990-43930999
13	BCL11A	chr15:43938746-43939054	GM12878	blood:	n/a	n/a
14	BCL11A	chr15:43982262-43982477	GM12878	blood:	n/a	n/a
15	BCLAF1	chr15:43930701-43931083	GM12878	blood:	n/a	chr15:43930990-43930999
16	BHLHE40	chr15:43939045-43939348	GM12878	blood:	n/a	n/a
17	CBX3	chr15:43982138-43982749	K562	blood:	n/a	chr15:43982622-43982633
18	CBX3	chr15:43982182-43982556	K562	blood:	n/a	n/a
19	CBX3	chr15:43985411-43986004	K562	blood:	n/a	n/a
20	CEBPB	chr15:43982162-43982682	GM12878	blood:	n/a	n/a
21	CEBPB	chr15:43914526-43914540	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr15:43894468-43894801	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr15:43913566-43913782	HepG2	liver:	n/a	chr15:43913662-43913673
24	CEBPB	chr15:43913554-43913750	K562	blood:	n/a	chr15:43913662-43913673
25	CEBPB	chr15:43933963-43933971	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr15:43933839-43934039	K562	blood:	n/a	n/a
27	CEBPD	chr15:43962726-43963199	K562	blood:	n/a	n/a
28	CHD2	chr15:43894517-43894780	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr15:43931127-43931189	GM12878	blood:	n/a	n/a
30	CTCF	chr15:43941291-43941369	Pancreas_OC	pancreas:	n/a	n/a
31	CTCF	chr15:43981816-43981820	GM19239	blood:	n/a	n/a
32	CTCF	chr15:43982161-43982505	K562	blood:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
33	CTCF	chr15:43898257-43898297	LNCaP	prostate:	n/a	n/a
34	CTCF	chr15:43982015-43982073	Lung_OC	lung:	n/a	n/a
35	CTCF	chr15:43982219-43982507	MCF-7	breast:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
36	CTCF	chr15:43982221-43982517	HUVEC	blood vessel:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
37	CTCF	chr15:43938709-43938821	Lung_OC	lung:	n/a	n/a
38	CTCF	chr15:43985492-43985500	GM13976	blood:	n/a	n/a
39	CTCF	chr15:43981755-43981812	GM19239	blood:	n/a	n/a
40	CTCF	chr15:43982197-43982582	Kidney_OC	kidney:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
41	CTCF	chr15:43903598-43903709	GM12878	blood:	n/a	n/a
42	CTCF	chr15:43982194-43982490	MCF-7	breast:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
43	CTCF	chr15:43982202-43982515	A549	lung:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
44	CTCF	chr15:43982181-43982538	Spleen_OC	spleen:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
45	CTCF	chr15:43982088-43982521	GM12892	blood:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
46	CTCF	chr15:43982174-43982513	NHEK	skin:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
47	CTCF	chr15:43982246-43982499	A549	lung:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372
48	CTCF	chr15:43969460-43969486	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr15:43982079-43982503	K562	blood:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
50	CTCF	chr15:43941291-43941401	GM12892	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:43942440-43942490	ProgFib	skin:	n/a
2	chr15:43942440-43942490	ProgFib	skin:	n/a
3	chr15:43983306-43983356	HEK293	kidney:	embryo
4	chr15:43931742-43931792	HEEpiC	esophagus:	n/a
5	chr15:43941642-43941692	HCPEpiC	choroid plexus:	n/a
6	chr15:43942014-43942064	BE2_C	brain:	n/a
7	chr15:43941072-43941122	HUVEC	blood vessel:	n/a
8	chr15:43989074-43989124	HRE	kidney:	n/a
9	chr15:43983306-43983356	PANC-1	pancreas:	n/a
10	chr15:43941072-43941122	HPAEpiC	pulmonary alveolar:	n/a
11	chr15:43893898-43893948	ovcar-3	ovarian:	n/a
12	chr15:43989074-43989124	ovcar-3	ovarian:	n/a
13	chr15:43983306-43983356	NHDF-neo	bronchial:	n/a
14	chr15:43941871-43941921	GM12878	blood:	n/a
15	chr15:43983306-43983356	H1-hESC	embryonic stem cell:	embryo
16	chr15:43983306-43983356	HL-60	blood:	n/a
17	chr15:43991375-43991425	IMR90	lung:	fetal
18	chr15:43941034-43941084	HRPEpiC	eye:	n/a
19	chr15:43941407-43941457	HNPCEpiC	eye:	n/a
20	chr15:43937339-43937389	HIPEpiC	eye:	n/a
21	chr15:43942440-43942490	U87	brain:	n/a
22	chr15:43983306-43983356	SKMC	muscle:	n/a
23	chr15:43984922-43984972	NT2-D1	testis:	n/a
24	chr15:43942014-43942064	GM12878	blood:	n/a
25	chr15:43983306-43983356	PrEC	prostate:	n/a
26	chr15:43942014-43942064	AoSMC	blood vessel:	n/a
27	chr15:43941563-43941613	HCM	heart:	n/a
28	chr15:43984922-43984972	PrEC	prostate:	n/a
29	chr15:43893898-43893948	BJ	skin:	n/a
30	chr15:43941407-43941457	BE2_C	brain:	n/a
31	chr15:43989074-43989124	HCF	heart:	n/a
32	chr15:43991375-43991425	GM12878	blood:	n/a
33	chr15:43942440-43942490	GM12892	blood:	n/a
34	chr15:43989074-43989124	ProgFib	skin:	n/a
35	chr15:43941042-43941092	SK-N-SH_RA	brain:	n/a
36	chr15:43893898-43893948	SK-N-SH_RA	brain:	n/a
37	chr15:43937339-43937389	ovcar-3	ovarian:	n/a
38	chr15:43940867-43940917	ECC-1	luminal epithelium:	n/a
39	chr15:43912221-43912271	GM12878	blood:	n/a
40	chr15:43941871-43941921	LNCaP	prostate:	n/a
41	chr15:43940140-43940190	CMK	blood:	n/a
42	chr15:43912221-43912271	MCF-7	breast:	n/a
43	chr15:43940867-43940917	BE2_C	brain:	n/a
44	chr15:43991375-43991425	HCPEpiC	choroid plexus:	n/a
45	chr15:43942014-43942064	MCF10A-Er-Src	breast:	n/a
46	chr15:43912221-43912271	ProgFib	skin:	n/a
47	chr15:43991375-43991425	AG10803	skin:	n/a
48	chr15:43984922-43984972	PANC-1	pancreas:	n/a
49	chr15:43941407-43941457	H1-hESC	embryonic stem cell:	embryo
50	chr15:43942014-43942064	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	15:43916541-43924442..15:44034348-44042259	K562	blood:
2	chr15:43946007..43947781-chr15:43949371..43952173,2	K562	blood:
3	15:43916541-43924442..15:44080886-44089111	GM12878	blood:
4	15:43792489-43802874..15:43916541-43924442	Hela-S3	cervix:
5	15:43889977-43895899..15:44001645-44015047	GM12878	blood:
6	15:43782117-43785993..15:43931042-43936532	GM12878	blood:
7	chr15:43946007..43947781-chr15:43949371..43952173,2	K562	blood:
8	15:43924442-43930824..15:44001645-44015047	GM12878	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TP53BP1-5	chr15:43924915-43925417	NONHSAT042101
2	lnc-TP53BP1-5	chr15:43924469-43924561	NONHSAT042101
3	lnc-MAP1A-1	chr15:43896982-43897099	ENSG00000240430.1

Variant related genes	Relation type
RNU6-353P	TF binding region
CATSPER2	TF binding region
PDIA3P2	TF binding region
RNU6-554P	TF binding region
STRC	TF binding region
RNU6-610P	TF binding region
CKMT1A	TF binding region
ENSG00000249839	TF binding region
ENSG00000238535	TF binding region
RNU6-353P	CpG island
CATSPER2	CpG island
PDIA3P2	CpG island
RNU6-554P	CpG island
STRC	CpG island
RNU6-610P	CpG island
CKMT1A	CpG island
ENSG00000249839	CpG island
ENSG00000238535	CpG island
ENSG00000140264	chromatin interactions
ENSG00000242028	chromatin interactions
ENSG00000167004	chromatin interactions
ENSG00000067369	chromatin interactions
ENSG00000242866	chromatin interactions
ENSG00000166763	chromatin interactions
ENSG00000238494	chromatin interactions
ENSG00000205771	chromatin interactions
ENSG00000221792	chromatin interactions

Extended variants
information (count: 2238 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:2238 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3097773	chr15:43893072-43893073	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs193034976	chr15:43893104-43893105	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs562392825	chr15:43893109-43893110	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs370775837	chr15:43893110-43893111	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs376833038	chr15:43893117-43893118	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs201290343	chr15:43893144-43893145	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs147963245	chr15:43893149-43893150	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs35527798	chr15:43893156-43893157	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs530869601	chr15:43893158-43893159	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs371120929	chr15:43893170-43893171	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs550671272	chr15:43893172-43893173	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs372949586	chr15:43893173-43893174	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs371263304	chr15:43893215-43893216	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs536673579	chr15:43893226-43893227	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs201699539	chr15:43893271-43893272	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs57893955	chr15:43893273-43893274	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs546707875	chr15:43893280-43893281	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs559396062	chr15:43893293-43893294	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs567143586	chr15:43893297-43893298	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs539385664	chr15:43893313-43893314	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs559148364	chr15:43893321-43893322	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs2614845	chr15:43893357-43893358	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs569481953	chr15:43893417-43893418	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs548985100	chr15:43893435-43893436	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs537904474	chr15:43893456-43893457	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs185244648	chr15:43893457-43893458	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs574474004	chr15:43893462-43893463	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs112768174	chr15:43893466-43893467	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs112602815	chr15:43893476-43893477	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs2614846	chr15:43893485-43893486	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs189735813	chr15:43893511-43893512	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs369886929	chr15:43893570-43893571	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs576724498	chr15:43893571-43893572	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs373763779	chr15:43893579-43893580	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs376627636	chr15:43893582-43893583	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs370674238	chr15:43893585-43893586	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs367738465	chr15:43893590-43893591	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs199839039	chr15:43893593-43893594	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs200698944	chr15:43893598-43893599	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs141809944	chr15:43893602-43893603	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs145567817	chr15:43893610-43893611	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs572743537	chr15:43893612-43893613	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs371525796	chr15:43893613-43893614	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs147717802	chr15:43893620-43893621	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs201929905	chr15:43893640-43893641	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs148862690	chr15:43893669-43893670	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs77493867	chr15:43893673-43893674	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs143487165	chr15:43893693-43893694	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs201633242	chr15:43893702-43893703	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs530174282	chr15:43893724-43893725	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
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	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
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	23813976	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:281 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43871400-43898000	Weak transcription	Gastric	stomach
2	chr15:43887400-43894200	Weak transcription	Placenta	Placenta
3	chr15:43887400-43894400	Weak transcription	Colonic Mucosa	Colon
4	chr15:43887400-43894400	Weak transcription	HMEC	breast
5	chr15:43887400-43894400	Weak transcription	NHEK	skin
6	chr15:43887600-43894000	Weak transcription	Rectal Smooth Muscle	rectum
7	chr15:43888200-43894400	Weak transcription	Esophagus	oesophagus
8	chr15:43889200-43893600	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr15:43889400-43894800	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr15:43890000-43894400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr15:43890000-43894400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr15:43890400-43894400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr15:43891400-43894400	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr15:43891600-43893600	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr15:43891600-43896600	Weak transcription	Duodenum Mucosa	Duodenum
16	chr15:43892000-43894400	Weak transcription	Fetal Intestine Small	intestine
17	chr15:43893000-43897200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr15:43893600-43893800	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr15:43893600-43894400	Enhancers	Hela-S3	cervix
20	chr15:43894200-43894600	Enhancers	Placenta	Placenta
21	chr15:43894200-43894800	Bivalent Enhancer	Fetal Muscle Leg	muscle
22	chr15:43894400-43894600	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr15:43894400-43894600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr15:43894400-43894600	Enhancers	Esophagus	oesophagus
25	chr15:43894400-43894600	Enhancers	NHEK	skin
26	chr15:43895400-43895600	Bivalent Enhancer	Fetal Muscle Leg	muscle
27	chr15:43913400-43914400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr15:43914000-43914400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr15:43914200-43914600	Enhancers	Fetal Intestine Small	intestine
30	chr15:43914600-43937400	Weak transcription	Fetal Intestine Small	intestine
31	chr15:43915000-43915400	Enhancers	Hela-S3	cervix
32	chr15:43915400-43941000	Weak transcription	Hela-S3	cervix
33	chr15:43917000-43918000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr15:43917200-43917800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr15:43917400-43918000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr15:43917600-43917800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr15:43919600-43941600	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr15:43920400-43941400	Weak transcription	Brain Hippocampus Middle	brain
39	chr15:43921000-43940600	Weak transcription	Gastric	stomach
40	chr15:43921400-43950400	Weak transcription	Aorta	Aorta
41	chr15:43921800-43952600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr15:43922200-43922600	Enhancers	Placenta	Placenta
43	chr15:43922800-43937600	Weak transcription	Fetal Intestine Large	intestine
44	chr15:43923200-43937400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr15:43923200-43951800	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr15:43924200-43924800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr15:43925200-43939200	Weak transcription	Brain Angular Gyrus	brain
48	chr15:43925200-43939800	Weak transcription	Brain Anterior Caudate	brain
49	chr15:43929600-43940200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr15:43929800-43937600	Weak transcription	Skeletal Muscle Male	skeletal muscle

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