Variant report

Variant	nsv534652
Chromosome Location	chr15:43851548-43948346
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:663)
CpG islands
(count:1343)
Chromatin interactive
region (count:7)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:663 , 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	chr15:43937824-43938301	GM12878	blood:	n/a	n/a
3	ATF2	chr15:43937873-43938217	GM12878	blood:	n/a	n/a
4	BATF	chr15:43937914-43938101	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	chr15:43931144-43931498	GM12878	blood:	n/a	n/a
8	BATF	chr15:43937842-43938114	GM12878	blood:	n/a	n/a
9	BATF	chr15:43882351-43882718	GM12878	blood:	n/a	n/a
10	BCL11A	chr15:43930652-43931058	GM12878	blood:	n/a	chr15:43930990-43930999
11	BCL11A	chr15:43938810-43938992	GM12878	blood:	n/a	n/a
12	BCL11A	chr15:43882430-43882645	GM12878	blood:	n/a	n/a
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	chr15:43882346-43882722	K562	blood:	n/a	n/a
21	CEBPB	chr15:43933963-43933971	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr15:43913554-43913750	K562	blood:	n/a	chr15:43913662-43913673
23	CEBPB	chr15:43913566-43913782	HepG2	liver:	n/a	chr15:43913662-43913673
24	CEBPB	chr15:43894468-43894801	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr15:43933839-43934039	K562	blood:	n/a	n/a
26	CEBPB	chr15:43914526-43914540	Hela-S3	cervix:	n/a	n/a
27	CEBPD	chr15:43882316-43882670	K562	blood:	n/a	n/a
28	CEBPD	chr15:43863161-43863508	K562	blood:	n/a	n/a
29	CHD2	chr15:43931127-43931189	GM12878	blood:	n/a	n/a
30	CHD2	chr15:43894517-43894780	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr15:43869920-43869924	MCF-7	breast:	n/a	n/a
32	CTCF	chr15:43904781-43904802	GM13977	blood:	n/a	n/a
33	CTCF	chr15:43941291-43941401	GM12892	blood:	n/a	n/a
34	CTCF	chr15:43941945-43942043	GM20000	blood:	n/a	n/a
35	CTCF	chr15:43882327-43882663	MCF-7	breast:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
36	CTCF	chr15:43882360-43882688	Kidney_OC	kidney:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
37	CTCF	chr15:43862177-43862207	GM10248	blood:	n/a	n/a
38	CTCF	chr15:43882328-43882673	MCF-7	breast:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
39	CTCF	chr15:43880578-43880609	HepG2	liver:	n/a	n/a
40	CTCF	chr15:43882379-43882684	Pancreas_OC	pancreas:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
41	CTCF	chr15:43882421-43882659	GM20000	blood:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
42	CTCF	chr15:43903384-43903840	K562	blood:	n/a	n/a
43	CTCF	chr15:43882414-43882667	A549	lung:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
44	CTCF	chr15:43856051-43856096	GM13976	blood:	n/a	n/a
45	CTCF	chr15:43941268-43941360	GM19240	blood:	n/a	n/a
46	CTCF	chr15:43882349-43882690	HepG2	liver:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
47	CTCF	chr15:43857288-43857401	GM13976	blood:	n/a	n/a
48	CTCF	chr15:43941284-43941422	GM19239	blood:	n/a	n/a
49	CTCF	chr15:43882348-43882717	Spleen_OC	spleen:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
50	CTCF	chr15:43922929-43922982	LNCaP	prostate:	n/a	n/a

(count:1343 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:43893898-43893948	CMK	blood:	n/a
2	chr15:43893898-43893948	CMK	blood:	n/a
3	chr15:43889864-43889914	A549	lung:	n/a
4	chr15:43891480-43891530	AG10803	skin:	n/a
5	chr15:43940140-43940190	GM12891	blood:	n/a
6	chr15:43883474-43883524	T-47D	breast:	n/a
7	chr15:43883469-43883519	HRE	kidney:	n/a
8	chr15:43941642-43941692	SK-N-SH	brain:	n/a
9	chr15:43942440-43942490	HMEC	breast:	n/a
10	chr15:43893898-43893948	GM19239	blood:	n/a
11	chr15:43883474-43883524	NHDF-neo	bronchial:	n/a
12	chr15:43941042-43941092	PANC-1	pancreas:	n/a
13	chr15:43883469-43883519	GM12892	blood:	n/a
14	chr15:43941042-43941092	MCF-7	breast:	n/a
15	chr15:43941642-43941692	Jurkat	blood:	n/a
16	chr15:43883469-43883519	U87	brain:	n/a
17	chr15:43940140-43940190	HIPEpiC	eye:	n/a
18	chr15:43941563-43941613	HCM	heart:	n/a
19	chr15:43889864-43889914	Hela-S3	cervix:	n/a
20	chr15:43940140-43940190	HL-60	blood:	n/a
21	chr15:43879335-43879385	PrEC	prostate:	n/a
22	chr15:43891480-43891530	HL-60	blood:	n/a
23	chr15:43889864-43889914	SK-N-MC	brain:	n/a
24	chr15:43942440-43942490	GM12878	blood:	n/a
25	chr15:43883469-43883519	HepG2	liver:	n/a
26	chr15:43941642-43941692	GM12892	blood:	n/a
27	chr15:43931742-43931792	RPTEC	kidney:	n/a
28	chr15:43883469-43883519	SAEC	small airway:	n/a
29	chr15:43885090-43885140	MCF10A-Er-Src	breast:	n/a
30	chr15:43940867-43940917	NHBE	bronchial:	n/a
31	chr15:43893898-43893948	RPTEC	kidney:	n/a
32	chr15:43891480-43891530	HEK293	kidney:	embryo
33	chr15:43941871-43941921	HCF	heart:	n/a
34	chr15:43941072-43941122	GM12891	blood:	n/a
35	chr15:43942014-43942064	HPAEpiC	pulmonary alveolar:	n/a
36	chr15:43937339-43937389	LNCaP	prostate:	n/a
37	chr15:43941034-43941084	HEK293	kidney:	embryo
38	chr15:43941563-43941613	IMR90	lung:	fetal
39	chr15:43880680-43880730	LNCaP	prostate:	n/a
40	chr15:43889864-43889914	AG10803	skin:	n/a
41	chr15:43889864-43889914	HMEC	breast:	n/a
42	chr15:43940867-43940917	IMR90	lung:	fetal
43	chr15:43942440-43942490	LNCaP	prostate:	n/a
44	chr15:43942014-43942064	BJ	skin:	n/a
45	chr15:43885090-43885140	Jurkat	blood:	n/a
46	chr15:43931742-43931792	LNCaP	prostate:	n/a
47	chr15:43941042-43941092	HUVEC	blood vessel:	n/a
48	chr15:43940140-43940190	CMK	blood:	n/a
49	chr15:43942014-43942064	AG09319	gingival:	n/a
50	chr15:43885090-43885140	BJ	skin:	n/a

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

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

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

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

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
ENSG00000166763	chromatin interactions
ENSG00000221792	chromatin interactions
ENSG00000238494	chromatin interactions
ENSG00000242866	chromatin interactions
ENSG00000140264	chromatin interactions
ENSG00000242028	chromatin interactions
ENSG00000167004	chromatin interactions
ENSG00000067369	chromatin interactions
ENSG00000205771	chromatin interactions

Extended variants
information (count: 2140 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:2140 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556935781	chr15:43851564-43851565	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs186324422	chr15:43851578-43851579	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs372915461	chr15:43851632-43851633	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs375915370	chr15:43851634-43851635	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs573358782	chr15:43851638-43851639	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs545249948	chr15:43851651-43851652	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553189733	chr15:43851652-43851653	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs565508938	chr15:43851712-43851713	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs574814273	chr15:43851722-43851723	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs191232721	chr15:43851805-43851806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544327284	chr15:43851833-43851834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs560826072	chr15:43851895-43851896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs2444245	chr15:43852043-43852044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs529728199	chr15:43852113-43852114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs144754493	chr15:43852148-43852149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs546886810	chr15:43852159-43852160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs566629688	chr15:43852162-43852163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs373024637	chr15:43852165-43852166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs138273725	chr15:43852496-43852497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs532469052	chr15:43852611-43852612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs552081040	chr15:43852624-43852625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs569082822	chr15:43852644-43852645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537102487	chr15:43852718-43852719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200420187	chr15:43852825-43852826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143869999	chr15:43853068-43853069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs557046289	chr15:43853069-43853070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs16952591	chr15:43853127-43853128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs139724685	chr15:43853145-43853146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs200455895	chr15:43853162-43853163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs368696446	chr15:43853163-43853164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs567289649	chr15:43853179-43853180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374455165	chr15:43853196-43853197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373042079	chr15:43853216-43853217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200932430	chr15:43853281-43853282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs59299708	chr15:43853330-43853331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs57651839	chr15:43853332-43853333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs59416777	chr15:43853434-43853435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558928743	chr15:43853438-43853439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs55827475	chr15:43853444-43853445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs59162745	chr15:43853450-43853451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147317103	chr15:43853462-43853463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs55779334	chr15:43853491-43853492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs58287887	chr15:43853504-43853505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs56275933	chr15:43853541-43853542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs56139860	chr15:43853545-43853546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200978226	chr15:43853590-43853591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141032391	chr15:43853591-43853592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549260588	chr15:43853596-43853597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs59206750	chr15:43853603-43853604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2614838	chr15:43853645-43853646	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:334 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43818000-43852600	Weak transcription	Rectal Smooth Muscle	rectum
2	chr15:43818200-43851600	Weak transcription	Primary hematopoietic stem cells	blood
3	chr15:43823800-43852600	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr15:43824800-43853000	Weak transcription	GM12878-XiMat	blood
5	chr15:43824800-43853200	Weak transcription	Hela-S3	cervix
6	chr15:43827400-43852600	Weak transcription	Left Ventricle	heart
7	chr15:43827400-43854000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr15:43827600-43851800	Weak transcription	Primary B cells from peripheral blood	blood
9	chr15:43827600-43852800	Weak transcription	Lung	lung
10	chr15:43827600-43854000	Weak transcription	Aorta	Aorta
11	chr15:43827600-43855400	Weak transcription	Ovary	ovary
12	chr15:43827800-43851600	Weak transcription	Thymus	Thymus
13	chr15:43827800-43852800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr15:43829000-43852600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr15:43839800-43853000	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr15:43840200-43852600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr15:43840200-43853200	Weak transcription	HMEC	breast
18	chr15:43840400-43851800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
19	chr15:43840800-43853200	Weak transcription	Psoas Muscle	Psoas
20	chr15:43842000-43852600	Weak transcription	NHEK	skin
21	chr15:43843200-43852600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr15:43843400-43852400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr15:43843400-43852600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr15:43845000-43852400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr15:43845200-43851800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr15:43847200-43853000	Weak transcription	Fetal Muscle Leg	muscle
27	chr15:43848400-43851800	Strong transcription	Brain Inferior Temporal Lobe	brain
28	chr15:43848600-43851600	Strong transcription	Sigmoid Colon	Sigmoid Colon
29	chr15:43848600-43851600	Strong transcription	Skeletal Muscle Female	skeletal muscle
30	chr15:43848600-43851800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr15:43848800-43851800	Strong transcription	Fetal Brain Female	brain
32	chr15:43848800-43851800	Strong transcription	Skeletal Muscle Male	skeletal muscle
33	chr15:43849000-43851800	Strong transcription	Rectal Mucosa Donor 29	rectum
34	chr15:43849200-43852000	Weak transcription	Brain Substantia Nigra	brain
35	chr15:43849200-43852600	Weak transcription	Liver	Liver
36	chr15:43849400-43852800	Weak transcription	Fetal Intestine Large	intestine
37	chr15:43849600-43851800	Strong transcription	Duodenum Mucosa	Duodenum
38	chr15:43849800-43852600	Weak transcription	Spleen	Spleen
39	chr15:43849800-43853200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr15:43849800-43853200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr15:43850000-43852600	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr15:43850000-43857000	Weak transcription	Brain Angular Gyrus	brain
43	chr15:43850200-43852600	Weak transcription	Brain Hippocampus Middle	brain
44	chr15:43850400-43851600	Strong transcription	Brain Cingulate Gyrus	brain
45	chr15:43850600-43851800	Strong transcription	Brain Germinal Matrix	brain
46	chr15:43851000-43851600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr15:43851200-43852800	Weak transcription	Primary T helper cells PMA-I stimulated	--
48	chr15:43851200-43852800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr15:43851200-43852800	Weak transcription	Colonic Mucosa	Colon
50	chr15:43851200-43852800	Weak transcription	Rectal Mucosa Donor 31	rectum

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