Variant report

Variant	nsv1514
Chromosome Location	chr15:43859260-43996580
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1004)
CpG islands
(count:1588)
Chromatin interactive
region (count:9)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1004 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr15:43930649-43931067	GM12878	blood:	n/a	n/a
2	ATF2	chr15:43937824-43938301	GM12878	blood:	n/a	n/a
3	ATF2	chr15:43937873-43938217	GM12878	blood:	n/a	n/a
4	BATF	chr15:43937842-43938114	GM12878	blood:	n/a	n/a
5	BATF	chr15:43882351-43882718	GM12878	blood:	n/a	n/a
6	BATF	chr15:43937914-43938101	GM12878	blood:	n/a	n/a
7	BATF	chr15:43930739-43931096	GM12878	blood:	n/a	n/a
8	BATF	chr15:43931124-43931473	GM12878	blood:	n/a	n/a
9	BATF	chr15:43982183-43982550	GM12878	blood:	n/a	n/a
10	BATF	chr15:43931144-43931498	GM12878	blood:	n/a	n/a
11	BCL11A	chr15:43982262-43982477	GM12878	blood:	n/a	n/a
12	BCL11A	chr15:43938746-43939054	GM12878	blood:	n/a	n/a
13	BCL11A	chr15:43938810-43938992	GM12878	blood:	n/a	n/a
14	BCL11A	chr15:43930652-43931058	GM12878	blood:	n/a	chr15:43930990-43930999
15	BCL11A	chr15:43930706-43930979	GM12878	blood:	n/a	n/a
16	BCL11A	chr15:43882430-43882645	GM12878	blood:	n/a	n/a
17	BCLAF1	chr15:43930701-43931083	GM12878	blood:	n/a	chr15:43930990-43930999
18	BHLHE40	chr15:43939045-43939348	GM12878	blood:	n/a	n/a
19	CBX3	chr15:43885528-43886169	K562	blood:	n/a	n/a
20	CBX3	chr15:43982182-43982556	K562	blood:	n/a	n/a
21	CBX3	chr15:43982138-43982749	K562	blood:	n/a	chr15:43982622-43982633
22	CBX3	chr15:43882308-43883030	K562	blood:	n/a	chr15:43882790-43882801
23	CBX3	chr15:43985411-43986004	K562	blood:	n/a	n/a
24	CBX3	chr15:43885781-43886051	K562	blood:	n/a	n/a
25	CEBPB	chr15:43913554-43913750	K562	blood:	n/a	chr15:43913662-43913673
26	CEBPB	chr15:43933963-43933971	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr15:43933839-43934039	K562	blood:	n/a	n/a
28	CEBPB	chr15:43894468-43894801	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr15:43914526-43914540	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr15:43882346-43882722	K562	blood:	n/a	n/a
31	CEBPB	chr15:43913566-43913782	HepG2	liver:	n/a	chr15:43913662-43913673
32	CEBPB	chr15:43982162-43982682	GM12878	blood:	n/a	n/a
33	CEBPD	chr15:43882316-43882670	K562	blood:	n/a	n/a
34	CEBPD	chr15:43863161-43863508	K562	blood:	n/a	n/a
35	CEBPD	chr15:43962726-43963199	K562	blood:	n/a	n/a
36	CHD2	chr15:43931127-43931189	GM12878	blood:	n/a	n/a
37	CHD2	chr15:43894517-43894780	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr15:43869920-43869924	MCF-7	breast:	n/a	n/a
39	CTCF	chr15:43882376-43882702	K562	blood:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
40	CTCF	chr15:43969462-43969553	MCF-7	breast:	n/a	n/a
41	CTCF	chr15:43864008-43864069	HepG2	liver:	n/a	n/a
42	CTCF	chr15:43982193-43982515	GM19240	blood:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
43	CTCF	chr15:43982204-43982517	MCF-7	breast:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
44	CTCF	chr15:43982174-43982513	NHEK	skin:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
45	CTCF	chr15:43982206-43982501	LNCaP	prostate:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
46	CTCF	chr15:43941291-43941401	GM12892	blood:	n/a	n/a
47	CTCF	chr15:43941258-43941416	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr15:43941276-43941415	MCF-7	breast:	n/a	n/a
49	CTCF	chr15:43985780-43985794	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr15:43869947-43869954	MCF-7	breast:	n/a	n/a

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:43991375-43991425	HIPEpiC	eye:	n/a
2	chr15:43885090-43885140	LNCaP	prostate:	n/a
3	chr15:43991375-43991425	HIPEpiC	eye:	n/a
4	chr15:43885090-43885140	LNCaP	prostate:	n/a
5	chr15:43991375-43991425	HRE	kidney:	n/a
6	chr15:43989074-43989124	NHDF-neo	bronchial:	n/a
7	chr15:43880680-43880730	RPTEC	kidney:	n/a
8	chr15:43880680-43880730	HL-60	blood:	n/a
9	chr15:43941034-43941084	HCPEpiC	choroid plexus:	n/a
10	chr15:43941407-43941457	AG04450	lung:	fetal
11	chr15:43989074-43989124	BJ	skin:	n/a
12	chr15:43931742-43931792	GM06990	blood:	n/a
13	chr15:43941563-43941613	Caco-2	colon:	n/a
14	chr15:43941072-43941122	HCM	heart:	n/a
15	chr15:43879335-43879385	AG09309	skin:	n/a
16	chr15:43940867-43940917	SK-N-SH_RA	brain:	n/a
17	chr15:43941072-43941122	GM06990	blood:	n/a
18	chr15:43883474-43883524	ECC-1	luminal epithelium:	n/a
19	chr15:43941072-43941122	HCF	heart:	n/a
20	chr15:43942440-43942490	SK-N-MC	brain:	n/a
21	chr15:43942014-43942064	H1-hESC	embryonic stem cell:	embryo
22	chr15:43893898-43893948	ovcar-3	ovarian:	n/a
23	chr15:43942440-43942490	H1-hESC	embryonic stem cell:	embryo
24	chr15:43885090-43885140	ovcar-3	ovarian:	n/a
25	chr15:43912221-43912271	SKMC	muscle:	n/a
26	chr15:43991375-43991425	AG04450	lung:	fetal
27	chr15:43941072-43941122	AG04449	skin:	fetal
28	chr15:43940140-43940190	NH-A	brain:	n/a
29	chr15:43883469-43883519	SK-N-MC	brain:	n/a
30	chr15:43984922-43984972	GM06990	blood:	n/a
31	chr15:43931742-43931792	HCF	heart:	n/a
32	chr15:43883469-43883519	HEEpiC	esophagus:	n/a
33	chr15:43942440-43942490	GM12892	blood:	n/a
34	chr15:43991375-43991425	NHDF-neo	bronchial:	n/a
35	chr15:43941042-43941092	SK-N-MC	brain:	n/a
36	chr15:43989074-43989124	GM12891	blood:	n/a
37	chr15:43941072-43941122	IMR90	lung:	fetal
38	chr15:43941871-43941921	MCF-7	breast:	n/a
39	chr15:43940140-43940190	SK-N-SH	brain:	n/a
40	chr15:43983306-43983356	BE2_C	brain:	n/a
41	chr15:43983306-43983356	GM12892	blood:	n/a
42	chr15:43989074-43989124	HL-60	blood:	n/a
43	chr15:43941072-43941122	RPTEC	kidney:	n/a
44	chr15:43940140-43940190	HCF	heart:	n/a
45	chr15:43941871-43941921	SKMC	muscle:	n/a
46	chr15:43941642-43941692	H1-hESC	embryonic stem cell:	embryo
47	chr15:43942440-43942490	HRE	kidney:	n/a
48	chr15:43931742-43931792	Jurkat	blood:	n/a
49	chr15:43983306-43983356	HEEpiC	esophagus:	n/a
50	chr15:43989074-43989124	HEK293	kidney:	embryo

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	15:43782117-43785993..15:43931042-43936532	GM12878	blood:
2	chr15:43946007..43947781-chr15:43949371..43952173,2	K562	blood:
3	15:43924442-43930824..15:44001645-44015047	GM12878	blood:
4	chr15:43946007..43947781-chr15:43949371..43952173,2	K562	blood:
5	15:43916541-43924442..15:44034348-44042259	K562	blood:
6	15:43792489-43802874..15:43916541-43924442	Hela-S3	cervix:
7	15:43889977-43895899..15:44001645-44015047	GM12878	blood:
8	15:43916541-43924442..15:44080886-44089111	GM12878	blood:
9	chr15:43821060..43823469-chr15:43995355..43996867,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CKMT1A-1	chr15:43886217-43886565	NONHSAT042092
2	lnc-TP53BP1-5	chr15:43924469-43924561	NONHSAT042101
3	lnc-TP53BP1-5	chr15:43924915-43925417	NONHSAT042101
4	lnc-MAP1A-1	chr15:43891590-43891731	ENSG00000240430.1
5	lnc-CKMT1A-1	chr15:43886243-43886620	NONHSAT042090
6	lnc-CKMT1A-1	chr15:43885406-43885469	NONHSAT042091
7	lnc-CKMT1A-1	chr15:43886893-43887142	NONHSAT042092
8	lnc-MAP1A-1	chr15:43896982-43897099	ENSG00000240430.1
9	lnc-CKMT1A-1	chr15:43885285-43885469	NONHSAT042090
10	lnc-CKMT1A-1	chr15:43886243-43886565	NONHSAT042091
11	lnc-CKMT1A-1	chr15:43886893-43887305	NONHSAT042091

No data

Variant related genes	Relation type
CATSPER2	TF binding region
PDIA3P2	TF binding region
STRC	TF binding region
RNU6-610P	TF binding region
CKMT1A	TF binding region
CKMT1B	TF binding region
ENSG00000249839	TF binding region
ENSG00000238535	TF binding region
RNU6-353P	TF binding region
RNU6-554P	TF binding region
PPIP5K1	TF binding region
CATSPER2	CpG island
PDIA3P2	CpG island
STRC	CpG island
RNU6-610P	CpG island
CKMT1A	CpG island
CKMT1B	CpG island
ENSG00000249839	CpG island
ENSG00000238535	CpG island
RNU6-353P	CpG island
RNU6-554P	CpG island
PPIP5K1	CpG island
ENSG00000242866	chromatin interactions
ENSG00000242028	chromatin interactions
ENSG00000067369	chromatin interactions
ENSG00000140264	chromatin interactions
ENSG00000166763	chromatin interactions
ENSG00000238494	chromatin interactions
ENSG00000221792	chromatin interactions
ENSG00000205771	chromatin interactions
ENSG00000167004	chromatin interactions

Extended variants
information (count: 2771 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:2771 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145958636	chr15:43859287-43859288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs148202516	chr15:43859317-43859318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs111698381	chr15:43859335-43859336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs372548480	chr15:43859401-43859402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs139876462	chr15:43859464-43859465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs143114460	chr15:43859536-43859537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs146667997	chr15:43859652-43859653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs140133719	chr15:43859778-43859779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs149956578	chr15:43859874-43859875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs145128593	chr15:43859932-43859933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs149076759	chr15:43860025-43860026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs143143622	chr15:43860137-43860138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs2288767	chr15:43860351-43860352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs142445902	chr15:43860694-43860695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs146645337	chr15:43861021-43861022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs139033756	chr15:43862694-43862695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141431474	chr15:43862784-43862785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs150477987	chr15:43862964-43862965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs138334859	chr15:43863053-43863054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs149606809	chr15:43863082-43863083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146123549	chr15:43863265-43863266	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs139843849	chr15:43863658-43863659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs141191158	chr15:43864469-43864470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201598736	chr15:43864550-43864551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs540215858	chr15:43864799-43864800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549116890	chr15:43864852-43864853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560132408	chr15:43864899-43864900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532305183	chr15:43864905-43864906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs552450890	chr15:43865138-43865139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs62018885	chr15:43866329-43866330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs141626144	chr15:43866361-43866362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs2447223	chr15:43867840-43867841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs148398780	chr15:43868596-43868597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs142518808	chr15:43870713-43870714	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs150737493	chr15:43870734-43870735	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs562506471	chr15:43870837-43870838	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs151002945	chr15:43870901-43870902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200799351	chr15:43871577-43871578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569183470	chr15:43871580-43871581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371291746	chr15:43871581-43871582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs180738137	chr15:43871632-43871633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs9652445	chr15:43871829-43871830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2915789	chr15:43871831-43871832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs9652446	chr15:43871851-43871852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs78551708	chr15:43871853-43871854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs2915790	chr15:43871863-43871864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375777382	chr15:43872513-43872514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200448556	chr15:43872584-43872585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs62018886	chr15:43872719-43872720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531420423	chr15:43872750-43872751	Weak transcription	n/a	n/a	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:326 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43851800-43889600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr15:43866000-43873600	Weak transcription	Brain Angular Gyrus	brain
3	chr15:43871400-43898000	Weak transcription	Gastric	stomach
4	chr15:43885000-43885200	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr15:43885000-43885200	Active TSS	Duodenum Mucosa	Duodenum
6	chr15:43885000-43885200	Active TSS	Rectal Mucosa Donor 29	rectum
7	chr15:43885000-43885200	Enhancers	K562	blood
8	chr15:43885200-43888600	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr15:43885200-43889800	Weak transcription	Duodenum Mucosa	Duodenum
10	chr15:43885400-43886200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr15:43887000-43888600	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr15:43887000-43888800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr15:43887200-43888800	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr15:43887200-43888800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr15:43887400-43889600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr15:43887400-43892800	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr15:43887400-43894200	Weak transcription	Placenta	Placenta
18	chr15:43887400-43894400	Weak transcription	Colonic Mucosa	Colon
19	chr15:43887400-43894400	Weak transcription	HMEC	breast
20	chr15:43887400-43894400	Weak transcription	NHEK	skin
21	chr15:43887600-43894000	Weak transcription	Rectal Smooth Muscle	rectum
22	chr15:43887800-43890200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr15:43888200-43889800	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr15:43888200-43894400	Weak transcription	Esophagus	oesophagus
25	chr15:43888600-43889400	Strong transcription	Rectal Mucosa Donor 29	rectum
26	chr15:43888600-43891600	Strong transcription	Rectal Mucosa Donor 31	rectum
27	chr15:43888800-43889200	Strong transcription	H9 Cell Line	embryonic stem cell
28	chr15:43888800-43890000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
29	chr15:43888800-43890400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr15:43889200-43891800	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr15:43889200-43893600	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr15:43889400-43894800	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr15:43889600-43890000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr15:43889600-43891200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr15:43889800-43890200	Strong transcription	Duodenum Mucosa	Duodenum
36	chr15:43889800-43890400	Strong transcription	HUES48 Cell Line	embryonic stem cell
37	chr15:43890000-43894400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr15:43890000-43894400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr15:43890200-43891000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr15:43890200-43891200	Weak transcription	Duodenum Mucosa	Duodenum
41	chr15:43890400-43890800	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr15:43890400-43894400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr15:43890800-43891400	Strong transcription	HUES48 Cell Line	embryonic stem cell
44	chr15:43891200-43891600	Strong transcription	Duodenum Mucosa	Duodenum
45	chr15:43891200-43892600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr15:43891400-43894400	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr15:43891600-43893600	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr15:43891600-43896600	Weak transcription	Duodenum Mucosa	Duodenum
49	chr15:43892000-43894400	Weak transcription	Fetal Intestine Small	intestine
50	chr15:43892600-43893000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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