Variant report

Variant	nsv904162
Chromosome Location	chr15:43873489-44011113
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	chr15:43930649-43931067	GM12878	blood:	n/a	n/a
2	ATF2	chr15:43937873-43938217	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	chr15:43882351-43882718	GM12878	blood:	n/a	n/a
6	BATF	chr15:43937842-43938114	GM12878	blood:	n/a	n/a
7	BATF	chr15:43931124-43931473	GM12878	blood:	n/a	n/a
8	BATF	chr15:43937914-43938101	GM12878	blood:	n/a	n/a
9	BATF	chr15:43930739-43931096	GM12878	blood:	n/a	n/a
10	BATF	chr15:43982183-43982550	GM12878	blood:	n/a	n/a
11	BCL11A	chr15:43938810-43938992	GM12878	blood:	n/a	n/a
12	BCL11A	chr15:43982262-43982477	GM12878	blood:	n/a	n/a
13	BCL11A	chr15:43882430-43882645	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	chr15:43938746-43939054	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	chr15:43885781-43886051	K562	blood:	n/a	n/a
20	CBX3	chr15:43982182-43982556	K562	blood:	n/a	n/a
21	CBX3	chr15:43885528-43886169	K562	blood:	n/a	n/a
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	chr15:43982138-43982749	K562	blood:	n/a	chr15:43982622-43982633
25	CEBPB	chr15:43913566-43913782	HepG2	liver:	n/a	chr15:43913662-43913673
26	CEBPB	chr15:43914526-43914540	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr15:43894468-43894801	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr15:43933963-43933971	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr15:43933839-43934039	K562	blood:	n/a	n/a
30	CEBPB	chr15:43982162-43982682	GM12878	blood:	n/a	n/a
31	CEBPB	chr15:43913554-43913750	K562	blood:	n/a	chr15:43913662-43913673
32	CEBPB	chr15:43882346-43882722	K562	blood:	n/a	n/a
33	CEBPD	chr15:43882316-43882670	K562	blood:	n/a	n/a
34	CEBPD	chr15:43962726-43963199	K562	blood:	n/a	n/a
35	CHD2	chr15:43931127-43931189	GM12878	blood:	n/a	n/a
36	CHD2	chr15:43894517-43894780	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr15:43982157-43982511	GM12891	blood:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
38	CTCF	chr15:43941276-43941415	MCF-7	breast:	n/a	n/a
39	CTCF	chr15:43882361-43882671	MCF-7	breast:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
40	CTCF	chr15:43882360-43882688	Kidney_OC	kidney:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
41	CTCF	chr15:43982182-43982515	GM19239	blood:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
42	CTCF	chr15:43882348-43882717	Spleen_OC	spleen:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
43	CTCF	chr15:43941279-43941373	HepG2	liver:	n/a	n/a
44	CTCF	chr15:43982203-43982544	GM10266	blood:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
45	CTCF	chr15:43982148-43982551	A549	lung:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
46	CTCF	chr15:43941262-43941391	GM12891	blood:	n/a	n/a
47	CTCF	chr15:43982246-43982499	A549	lung:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372
48	CTCF	chr15:43882382-43882682	ProgFib	skin:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
49	CTCF	chr15:43902588-43902631	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr15:43903384-43903840	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:43889864-43889914	MCF10A-Er-Src	breast:	n/a
2	chr15:43940140-43940190	H1-hESC	embryonic stem cell:	embryo
3	chr15:43889864-43889914	MCF10A-Er-Src	breast:	n/a
4	chr15:43940140-43940190	H1-hESC	embryonic stem cell:	embryo
5	chr15:43889864-43889914	AG04449	skin:	fetal
6	chr15:43942440-43942490	K562	blood:	n/a
7	chr15:43883474-43883524	HPAEpiC	pulmonary alveolar:	n/a
8	chr15:43880680-43880730	Caco-2	colon:	n/a
9	chr15:43983306-43983356	ovcar-3	ovarian:	n/a
10	chr15:43891480-43891530	NH-A	brain:	n/a
11	chr15:43991375-43991425	CMK	blood:	n/a
12	chr15:43912221-43912271	AG10803	skin:	n/a
13	chr15:43941034-43941084	SK-N-MC	brain:	n/a
14	chr15:43891480-43891530	PANC-1	pancreas:	n/a
15	chr15:43941407-43941457	HUVEC	blood vessel:	n/a
16	chr15:43889864-43889914	SKMC	muscle:	n/a
17	chr15:43941042-43941092	MCF10A-Er-Src	breast:	n/a
18	chr15:43880680-43880730	HNPCEpiC	eye:	n/a
19	chr15:43941042-43941092	HEEpiC	esophagus:	n/a
20	chr15:43941042-43941092	HPAEpiC	pulmonary alveolar:	n/a
21	chr15:43984922-43984972	Jurkat	blood:	n/a
22	chr15:43931742-43931792	PANC-1	pancreas:	n/a
23	chr15:43879335-43879385	PANC-1	pancreas:	n/a
24	chr15:43879335-43879385	ProgFib	skin:	n/a
25	chr15:43941871-43941921	ECC-1	luminal epithelium:	n/a
26	chr15:43983306-43983356	AG04449	skin:	fetal
27	chr15:43941407-43941457	A549	lung:	n/a
28	chr15:43879335-43879385	AG09319	gingival:	n/a
29	chr15:43984922-43984972	PFSK-1	brain:	n/a
30	chr15:43991375-43991425	NH-A	brain:	n/a
31	chr15:43941034-43941084	RPTEC	kidney:	n/a
32	chr15:43941407-43941457	GM12878	blood:	n/a
33	chr15:43879335-43879385	HCT-116	colon:	n/a
34	chr15:43983306-43983356	HCPEpiC	choroid plexus:	n/a
35	chr15:43983306-43983356	BE2_C	brain:	n/a
36	chr15:43984922-43984972	HEEpiC	esophagus:	n/a
37	chr15:43989074-43989124	GM19239	blood:	n/a
38	chr15:43941563-43941613	NH-A	brain:	n/a
39	chr15:43984922-43984972	T-47D	breast:	n/a
40	chr15:43941563-43941613	PrEC	prostate:	n/a
41	chr15:43989074-43989124	GM06990	blood:	n/a
42	chr15:43893898-43893948	Hepatocyte	liver:	n/a
43	chr15:43885090-43885140	SKMC	muscle:	n/a
44	chr15:43942014-43942064	H1-hESC	embryonic stem cell:	embryo
45	chr15:43941072-43941122	PANC-1	pancreas:	n/a
46	chr15:43989074-43989124	GM12878	blood:	n/a
47	chr15:43942014-43942064	Caco-2	colon:	n/a
48	chr15:43942014-43942064	GM12891	blood:	n/a
49	chr15:43984922-43984972	NB4	blood:	n/a
50	chr15:43941034-43941084	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	15:43792489-43802874..15:43916541-43924442	Hela-S3	cervix:
2	15:43889977-43895899..15:44001645-44015047	GM12878	blood:
3	15:44001645-44015047..15:44080886-44089111	Hela-S3	cervix:
4	15:43924442-43930824..15:44001645-44015047	GM12878	blood:
5	15:43916541-43924442..15:44034348-44042259	K562	blood:
6	15:43782117-43785993..15:44001645-44015047	GM12878	blood:
7	chr15:43946007..43947781-chr15:43949371..43952173,2	K562	blood:
8	chr15:43821060..43823469-chr15:43995355..43996867,2	K562	blood:
9	15:43889977-43895899..15:44001645-44015047	GM12878	blood:
10	15:43916541-43924442..15:44080886-44089111	GM12878	blood:
11	15:43792489-43802874..15:44001645-44015047	GM12878	blood:
12	15:43782117-43785993..15:43931042-43936532	GM12878	blood:
13	chr15:43946007..43947781-chr15:43949371..43952173,2	K562	blood:
14	15:43802874-43806906..15:44001645-44015047	Hela-S3	cervix:
15	15:43807815-43812531..15:44001645-44015047	Hela-S3	cervix:
16	15:43924442-43930824..15:44001645-44015047	GM12878	blood:

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

Variant related genes	Relation type
RNU6-353P	TF binding region
CATSPER2	TF binding region
ENSG00000238494	TF binding region
PDIA3P2	TF binding region
RNU6-554P	TF binding region
STRC	TF binding region
PPIP5K1	TF binding region
RNU6-610P	TF binding region
CKMT1A	TF binding region
STRCP1	TF binding region
CKMT1B	TF binding region
ENSG00000249839	TF binding region
ENSG00000238535	TF binding region
RNU6-353P	CpG island
CATSPER2	CpG island
ENSG00000238494	CpG island
PDIA3P2	CpG island
RNU6-554P	CpG island
STRC	CpG island
PPIP5K1	CpG island
RNU6-610P	CpG island
CKMT1A	CpG island
STRCP1	CpG island
CKMT1B	CpG island
ENSG00000249839	CpG island
ENSG00000238535	CpG island
ENSG00000166763	chromatin interactions
ENSG00000222398	chromatin interactions
ENSG00000140264	chromatin interactions
ENSG00000166963	chromatin interactions
ENSG00000242866	chromatin interactions
ENSG00000167004	chromatin interactions
ENSG00000067369	chromatin interactions
ENSG00000237289	chromatin interactions
ENSG00000205771	chromatin interactions
ENSG00000206991	chromatin interactions
ENSG00000242028	chromatin interactions
ENSG00000166762	chromatin interactions
ENSG00000238494	chromatin interactions
ENSG00000221792	chromatin interactions

Extended variants
information (count: 2896 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:2896 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373368300	chr15:43873490-43873491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs574572279	chr15:43873521-43873522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs368128606	chr15:43873528-43873529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs201054366	chr15:43873540-43873541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs145184127	chr15:43873543-43873544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs559850420	chr15:43873628-43873629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576783274	chr15:43873629-43873630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs545747307	chr15:43873647-43873648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562466177	chr15:43873662-43873663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531528956	chr15:43873667-43873668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547967672	chr15:43873676-43873677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561587123	chr15:43873696-43873697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530089131	chr15:43873742-43873743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs547080608	chr15:43873783-43873784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs566718157	chr15:43873807-43873808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539044645	chr15:43873838-43873839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs552314452	chr15:43873864-43873865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs147822206	chr15:43874252-43874253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569554742	chr15:43875435-43875436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs141385239	chr15:43875454-43875455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538575758	chr15:43875478-43875479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555195794	chr15:43875531-43875532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575091360	chr15:43875532-43875533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs62018887	chr15:43875837-43875838	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs62018888	chr15:43876097-43876098	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs146507774	chr15:43876922-43876923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs28557224	chr15:43877977-43877978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs371017360	chr15:43878045-43878046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533615096	chr15:43878056-43878057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs113119197	chr15:43878469-43878470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577536020	chr15:43878597-43878598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs375477880	chr15:43878898-43878899	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs2447224	chr15:43878907-43878908	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs139100270	chr15:43878947-43878948	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs553849693	chr15:43879078-43879079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs377663656	chr15:43879147-43879148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562258588	chr15:43879148-43879149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs142099435	chr15:43879154-43879155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576738857	chr15:43879380-43879381	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs545763209	chr15:43879751-43879752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562180621	chr15:43879752-43879753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575922779	chr15:43880598-43880599	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs148919372	chr15:43880632-43880633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs143666642	chr15:43883465-43883466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs62018889	chr15:43883573-43883574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs142013179	chr15:43884320-43884321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs145183678	chr15:43884456-43884457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138961594	chr15:43884635-43884636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs142174958	chr15:43884953-43884954	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs146202643	chr15:43884965-43884966	Weak transcription	TF binding region	2 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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:327 , 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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