Variant report

Variant	esv3506097
Chromosome Location	chr15:43853954-43953553
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:664)
CpG islands
(count:1345)
Chromatin interactive
region (count:8)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:664 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

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	chr15:43937842-43938114	GM12878	blood:	n/a	n/a
5	BATF	chr15:43931124-43931473	GM12878	blood:	n/a	n/a
6	BATF	chr15:43937914-43938101	GM12878	blood:	n/a	n/a
7	BATF	chr15:43931144-43931498	GM12878	blood:	n/a	n/a
8	BATF	chr15:43930739-43931096	GM12878	blood:	n/a	n/a
9	BATF	chr15:43882351-43882718	GM12878	blood:	n/a	n/a
10	BCL11A	chr15:43882430-43882645	GM12878	blood:	n/a	n/a
11	BCL11A	chr15:43938810-43938992	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	chr15:43930706-43930979	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	chr15:43882308-43883030	K562	blood:	n/a	chr15:43882790-43882801
18	CBX3	chr15:43885781-43886051	K562	blood:	n/a	n/a
19	CBX3	chr15:43885528-43886169	K562	blood:	n/a	n/a
20	CEBPB	chr15:43913566-43913782	HepG2	liver:	n/a	chr15:43913662-43913673
21	CEBPB	chr15:43882346-43882722	K562	blood:	n/a	n/a
22	CEBPB	chr15:43914526-43914540	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr15:43913554-43913750	K562	blood:	n/a	chr15:43913662-43913673
24	CEBPB	chr15:43933839-43934039	K562	blood:	n/a	n/a
25	CEBPB	chr15:43894468-43894801	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr15:43933963-43933971	Hela-S3	cervix:	n/a	n/a
27	CEBPD	chr15:43863161-43863508	K562	blood:	n/a	n/a
28	CEBPD	chr15:43882316-43882670	K562	blood:	n/a	n/a
29	CHD2	chr15:43894517-43894780	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr15:43931127-43931189	GM12878	blood:	n/a	n/a
31	CTCF	chr15:43882360-43882722	GM12878	blood:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
32	CTCF	chr15:43941258-43941416	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr15:43903384-43903840	K562	blood:	n/a	n/a
34	CTCF	chr15:43903507-43903768	K562	blood:	n/a	n/a
35	CTCF	chr15:43882376-43882702	K562	blood:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
36	CTCF	chr15:43941291-43941401	GM12892	blood:	n/a	n/a
37	CTCF	chr15:43903572-43903813	K562	blood:	n/a	n/a
38	CTCF	chr15:43882371-43882688	A549	lung:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
39	CTCF	chr15:43869860-43870007	MCF-7	breast:	n/a	n/a
40	CTCF	chr15:43859245-43859295	GM13977	blood:	n/a	n/a
41	CTCF	chr15:43857288-43857401	GM13976	blood:	n/a	n/a
42	CTCF	chr15:43880578-43880609	HepG2	liver:	n/a	n/a
43	CTCF	chr15:43882322-43882674	GM19239	blood:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
44	CTCF	chr15:43869930-43869937	MCF-7	breast:	n/a	n/a
45	CTCF	chr15:43903637-43903732	GM12892	blood:	n/a	n/a
46	CTCF	chr15:43941279-43941373	HepG2	liver:	n/a	n/a
47	CTCF	chr15:43882339-43882679	NHEK	skin:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
48	CTCF	chr15:43941268-43941360	GM19240	blood:	n/a	n/a
49	CTCF	chr15:43882421-43882659	GM20000	blood:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
50	CTCF	chr15:43941294-43941380	Hela-S3	cervix:	n/a	n/a

(count:1345 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:43880680-43880730	T-47D	breast:	n/a
2	chr15:43941642-43941692	NT2-D1	testis:	n/a
3	chr15:43937339-43937389	HNPCEpiC	eye:	n/a
4	chr15:43880680-43880730	T-47D	breast:	n/a
5	chr15:43941642-43941692	NT2-D1	testis:	n/a
6	chr15:43937339-43937389	HNPCEpiC	eye:	n/a
7	chr15:43893898-43893948	HRE	kidney:	n/a
8	chr15:43931742-43931792	BE2_C	brain:	n/a
9	chr15:43880680-43880730	ovcar-3	ovarian:	n/a
10	chr15:43941871-43941921	Jurkat	blood:	n/a
11	chr15:43937339-43937389	IMR90	lung:	fetal
12	chr15:43937339-43937389	HCPEpiC	choroid plexus:	n/a
13	chr15:43883474-43883524	HCT-116	colon:	n/a
14	chr15:43937339-43937389	MCF-7	breast:	n/a
15	chr15:43879335-43879385	SAEC	small airway:	n/a
16	chr15:43941563-43941613	HIPEpiC	eye:	n/a
17	chr15:43885090-43885140	BJ	skin:	n/a
18	chr15:43883469-43883519	HCT-116	colon:	n/a
19	chr15:43941563-43941613	RPTEC	kidney:	n/a
20	chr15:43941563-43941613	HRE	kidney:	n/a
21	chr15:43885090-43885140	A549	lung:	n/a
22	chr15:43941871-43941921	SK-N-SH_RA	brain:	n/a
23	chr15:43883474-43883524	AG04449	skin:	fetal
24	chr15:43940140-43940190	HEK293	kidney:	embryo
25	chr15:43941871-43941921	HCT-116	colon:	n/a
26	chr15:43879335-43879385	NT2-D1	testis:	n/a
27	chr15:43942440-43942490	HepG2	liver:	n/a
28	chr15:43883474-43883524	GM19239	blood:	n/a
29	chr15:43891480-43891530	GM06990	blood:	n/a
30	chr15:43937339-43937389	ProgFib	skin:	n/a
31	chr15:43937339-43937389	NB4	blood:	n/a
32	chr15:43941042-43941092	HIPEpiC	eye:	n/a
33	chr15:43941563-43941613	NB4	blood:	n/a
34	chr15:43941871-43941921	BE2_C	brain:	n/a
35	chr15:43880680-43880730	SKMC	muscle:	n/a
36	chr15:43889864-43889914	HCF	heart:	n/a
37	chr15:43941042-43941092	NHDF-neo	bronchial:	n/a
38	chr15:43937339-43937389	HMEC	breast:	n/a
39	chr15:43941563-43941613	GM12892	blood:	n/a
40	chr15:43941072-43941122	MCF-7	breast:	n/a
41	chr15:43879335-43879385	BJ	skin:	n/a
42	chr15:43942440-43942490	AG04450	lung:	fetal
43	chr15:43883469-43883519	HRE	kidney:	n/a
44	chr15:43912221-43912271	Jurkat	blood:	n/a
45	chr15:43941034-43941084	SAEC	small airway:	n/a
46	chr15:43941042-43941092	H1-hESC	embryonic stem cell:	embryo
47	chr15:43941407-43941457	HRCEpiC	kidney:	n/a
48	chr15:43941871-43941921	ovcar-3	ovarian:	n/a
49	chr15:43891480-43891530	SK-N-MC	brain:	n/a
50	chr15:43889864-43889914	BJ	skin:	n/a

(count:8 , 50 per page) page: 1

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TP53BP1-5	chr15:43924915-43925417	NONHSAT042101
2	lnc-CKMT1A-1	chr15:43886243-43886565	NONHSAT042091
3	lnc-CKMT1A-1	chr15:43885285-43885469	NONHSAT042090
4	lnc-CKMT1A-1	chr15:43886893-43887305	NONHSAT042091
5	lnc-MAP1A-1	chr15:43891590-43891731	ENSG00000240430.1
6	lnc-CKMT1A-1	chr15:43886243-43886620	NONHSAT042090
7	lnc-MAP1A-1	chr15:43896982-43897099	ENSG00000240430.1
8	lnc-CKMT1A-1	chr15:43886893-43887142	NONHSAT042092
9	lnc-CKMT1A-1	chr15:43886217-43886565	NONHSAT042092
10	lnc-TP53BP1-5	chr15:43924469-43924561	NONHSAT042101
11	lnc-CKMT1A-1	chr15:43885406-43885469	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
CKMT1B	TF binding region
ENSG00000238535	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
CKMT1B	CpG island
ENSG00000238535	CpG island
RNU6-554P	CpG island
PPIP5K1	CpG island
ENSG00000242866	chromatin interactions
ENSG00000167004	chromatin interactions
ENSG00000140264	chromatin interactions
ENSG00000067369	chromatin interactions
ENSG00000166763	chromatin interactions
ENSG00000238494	chromatin interactions
ENSG00000205771	chromatin interactions
ENSG00000221792	chromatin interactions
ENSG00000242028	chromatin interactions

Extended variants
information (count: 2239 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:2239 , 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	rs150881014	chr15:43854263-43854264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs139380695	chr15:43854299-43854300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs149904782	chr15:43854311-43854312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs144960499	chr15:43854326-43854327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs4146520	chr15:43854343-43854344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs143180995	chr15:43854494-43854495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs62018882	chr15:43854600-43854601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs140407111	chr15:43854602-43854603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs62018883	chr15:43854669-43854670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs62018884	chr15:43854674-43854675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544288578	chr15:43854900-43854901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2602137	chr15:43854978-43854979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs148031681	chr15:43855761-43855762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs143733706	chr15:43855845-43855846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs140845378	chr15:43855955-43855956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs150425217	chr15:43855968-43855969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs138406263	chr15:43857459-43857460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143808177	chr15:43857532-43857533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147246765	chr15:43857556-43857557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs139308392	chr15:43857638-43857639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs149429095	chr15:43857650-43857651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs28393787	chr15:43857668-43857669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560985483	chr15:43857740-43857741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529841114	chr15:43857744-43857745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533393915	chr15:43857750-43857751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs147137489	chr15:43857751-43857752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs113050399	chr15:43857768-43857769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs144866341	chr15:43859082-43859083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs148553603	chr15:43859243-43859244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs142940054	chr15:43859259-43859260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145958636	chr15:43859287-43859288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148202516	chr15:43859317-43859318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs111698381	chr15:43859335-43859336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372548480	chr15:43859401-43859402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs139876462	chr15:43859464-43859465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs143114460	chr15:43859536-43859537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146667997	chr15:43859652-43859653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140133719	chr15:43859778-43859779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs149956578	chr15:43859874-43859875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs145128593	chr15:43859932-43859933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs149076759	chr15:43860025-43860026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143143622	chr15:43860137-43860138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2288767	chr15:43860351-43860352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs142445902	chr15:43860694-43860695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146645337	chr15:43861021-43861022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs139033756	chr15:43862694-43862695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141431474	chr15:43862784-43862785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs150477987	chr15:43862964-43862965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138334859	chr15:43863053-43863054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs149606809	chr15:43863082-43863083	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:267 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43827400-43854000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr15:43827600-43854000	Weak transcription	Aorta	Aorta
3	chr15:43827600-43855400	Weak transcription	Ovary	ovary
4	chr15:43850000-43857000	Weak transcription	Brain Angular Gyrus	brain
5	chr15:43851200-43854000	Weak transcription	Fetal Intestine Small	intestine
6	chr15:43851400-43854600	Weak transcription	Stomach Smooth Muscle	stomach
7	chr15:43851800-43856600	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr15:43851800-43889600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr15:43866000-43873600	Weak transcription	Brain Angular Gyrus	brain
10	chr15:43871400-43898000	Weak transcription	Gastric	stomach
11	chr15:43885000-43885200	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr15:43885000-43885200	Active TSS	Duodenum Mucosa	Duodenum
13	chr15:43885000-43885200	Active TSS	Rectal Mucosa Donor 29	rectum
14	chr15:43885000-43885200	Enhancers	K562	blood
15	chr15:43885200-43888600	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr15:43885200-43889800	Weak transcription	Duodenum Mucosa	Duodenum
17	chr15:43885400-43886200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr15:43887000-43888600	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr15:43887000-43888800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr15:43887200-43888800	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr15:43887200-43888800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr15:43887400-43889600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr15:43887400-43892800	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr15:43887400-43894200	Weak transcription	Placenta	Placenta
25	chr15:43887400-43894400	Weak transcription	Colonic Mucosa	Colon
26	chr15:43887400-43894400	Weak transcription	HMEC	breast
27	chr15:43887400-43894400	Weak transcription	NHEK	skin
28	chr15:43887600-43894000	Weak transcription	Rectal Smooth Muscle	rectum
29	chr15:43887800-43890200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr15:43888200-43889800	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr15:43888200-43894400	Weak transcription	Esophagus	oesophagus
32	chr15:43888600-43889400	Strong transcription	Rectal Mucosa Donor 29	rectum
33	chr15:43888600-43891600	Strong transcription	Rectal Mucosa Donor 31	rectum
34	chr15:43888800-43889200	Strong transcription	H9 Cell Line	embryonic stem cell
35	chr15:43888800-43890000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chr15:43888800-43890400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr15:43889200-43891800	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr15:43889200-43893600	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr15:43889400-43894800	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr15:43889600-43890000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr15:43889600-43891200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr15:43889800-43890200	Strong transcription	Duodenum Mucosa	Duodenum
43	chr15:43889800-43890400	Strong transcription	HUES48 Cell Line	embryonic stem cell
44	chr15:43890000-43894400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr15:43890000-43894400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr15:43890200-43891000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr15:43890200-43891200	Weak transcription	Duodenum Mucosa	Duodenum
48	chr15:43890400-43890800	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr15:43890400-43894400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr15:43890800-43891400	Strong transcription	HUES48 Cell Line	embryonic stem cell

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