Variant report

Variant	nsv524910
Chromosome Location	chr15:43836478-43939642
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:535)
CpG islands
(count:674)
Chromatin interactive
region (count:8)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:535 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

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	chr15:43937824-43938301	GM12878	blood:	n/a	n/a
3	ATF2	chr15:43930649-43931067	GM12878	blood:	n/a	n/a
4	BATF	chr15:43937842-43938114	GM12878	blood:	n/a	n/a
5	BATF	chr15:43931144-43931498	GM12878	blood:	n/a	n/a
6	BATF	chr15:43931124-43931473	GM12878	blood:	n/a	n/a
7	BATF	chr15:43882351-43882718	GM12878	blood:	n/a	n/a
8	BATF	chr15:43930739-43931096	GM12878	blood:	n/a	n/a
9	BATF	chr15:43937914-43938101	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	chr15:43938746-43939054	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	BCLAF1	chr15:43930701-43931083	GM12878	blood:	n/a	chr15:43930990-43930999
16	BHLHE40	chr15:43939045-43939348	GM12878	blood:	n/a	n/a
17	CBX3	chr15:43885528-43886169	K562	blood:	n/a	n/a
18	CBX3	chr15:43882308-43883030	K562	blood:	n/a	chr15:43882790-43882801
19	CBX3	chr15:43885781-43886051	K562	blood:	n/a	n/a
20	CEBPB	chr15:43913566-43913782	HepG2	liver:	n/a	chr15:43913662-43913673
21	CEBPB	chr15:43933839-43934039	K562	blood:	n/a	n/a
22	CEBPB	chr15:43914526-43914540	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr15:43933963-43933971	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr15:43838707-43838732	K562	blood:	n/a	n/a
25	CEBPB	chr15:43913554-43913750	K562	blood:	n/a	chr15:43913662-43913673
26	CEBPB	chr15:43894468-43894801	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr15:43882346-43882722	K562	blood:	n/a	n/a
28	CEBPD	chr15:43882316-43882670	K562	blood:	n/a	n/a
29	CEBPD	chr15:43863161-43863508	K562	blood:	n/a	n/a
30	CHD2	chr15:43894517-43894780	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr15:43931127-43931189	GM12878	blood:	n/a	n/a
32	CTCF	chr15:43869853-43870012	K562	blood:	n/a	n/a
33	CTCF	chr15:43865432-43865594	GM13976	blood:	n/a	n/a
34	CTCF	chr15:43882348-43882700	GM19238	blood:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
35	CTCF	chr15:43882316-43882692	GM12892	blood:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
36	CTCF	chr15:43882096-43882133	GM19239	blood:	n/a	n/a
37	CTCF	chr15:43882327-43882663	MCF-7	breast:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
38	CTCF	chr15:43903608-43903750	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr15:43903572-43903813	K562	blood:	n/a	n/a
40	CTCF	chr15:43857288-43857401	GM13976	blood:	n/a	n/a
41	CTCF	chr15:43839012-43839055	GM10248	blood:	n/a	n/a
42	CTCF	chr15:43862177-43862207	GM10248	blood:	n/a	n/a
43	CTCF	chr15:43882247-43882764	K562	blood:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
44	CTCF	chr15:43855883-43855920	GM13976	blood:	n/a	n/a
45	CTCF	chr15:43869920-43869924	MCF-7	breast:	n/a	n/a
46	CTCF	chr15:43882377-43882668	GM13977	blood:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
47	CTCF	chr15:43926469-43926503	LNCaP	prostate:	n/a	n/a
48	CTCF	chr15:43861384-43861415	GM10248	blood:	n/a	n/a
49	CTCF	chr15:43869860-43870007	MCF-7	breast:	n/a	n/a
50	CTCF	chr15:43903384-43903840	K562	blood:	n/a	n/a

(count:674 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:43891480-43891530	SK-N-MC	brain:	n/a
2	chr15:43912221-43912271	GM06990	blood:	n/a
3	chr15:43879335-43879385	AoSMC	blood vessel:	n/a
4	chr15:43891480-43891530	SK-N-MC	brain:	n/a
5	chr15:43912221-43912271	GM06990	blood:	n/a
6	chr15:43879335-43879385	AoSMC	blood vessel:	n/a
7	chr15:43889864-43889914	SKMC	muscle:	n/a
8	chr15:43889864-43889914	T-47D	breast:	n/a
9	chr15:43937339-43937389	HL-60	blood:	n/a
10	chr15:43931742-43931792	HUVEC	blood vessel:	n/a
11	chr15:43889864-43889914	IMR90	lung:	fetal
12	chr15:43912221-43912271	HUVEC	blood vessel:	n/a
13	chr15:43893898-43893948	Caco-2	colon:	n/a
14	chr15:43891480-43891530	NB4	blood:	n/a
15	chr15:43879335-43879385	LNCaP	prostate:	n/a
16	chr15:43889864-43889914	HMEC	breast:	n/a
17	chr15:43891480-43891530	U87	brain:	n/a
18	chr15:43937339-43937389	GM06990	blood:	n/a
19	chr15:43937339-43937389	ovcar-3	ovarian:	n/a
20	chr15:43880680-43880730	PrEC	prostate:	n/a
21	chr15:43912221-43912271	AG04449	skin:	fetal
22	chr15:43885090-43885140	CMK	blood:	n/a
23	chr15:43893898-43893948	HRPEpiC	eye:	n/a
24	chr15:43912221-43912271	HEEpiC	esophagus:	n/a
25	chr15:43885090-43885140	AG09319	gingival:	n/a
26	chr15:43885090-43885140	PFSK-1	brain:	n/a
27	chr15:43883474-43883524	AG09309	skin:	n/a
28	chr15:43931742-43931792	Caco-2	colon:	n/a
29	chr15:43889864-43889914	AG10803	skin:	n/a
30	chr15:43883469-43883519	HepG2	liver:	n/a
31	chr15:43883474-43883524	U87	brain:	n/a
32	chr15:43885090-43885140	K562	blood:	n/a
33	chr15:43883474-43883524	HPAEpiC	pulmonary alveolar:	n/a
34	chr15:43883474-43883524	SKMC	muscle:	n/a
35	chr15:43891480-43891530	HEK293	kidney:	embryo
36	chr15:43937339-43937389	HRE	kidney:	n/a
37	chr15:43883474-43883524	RPTEC	kidney:	n/a
38	chr15:43883474-43883524	AoSMC	blood vessel:	n/a
39	chr15:43880680-43880730	HRCEpiC	kidney:	n/a
40	chr15:43883474-43883524	NB4	blood:	n/a
41	chr15:43891480-43891530	AG04450	lung:	fetal
42	chr15:43880680-43880730	Hela-S3	cervix:	n/a
43	chr15:43883474-43883524	SK-N-SH	brain:	n/a
44	chr15:43885090-43885140	A549	lung:	n/a
45	chr15:43889864-43889914	HRPEpiC	eye:	n/a
46	chr15:43893898-43893948	HNPCEpiC	eye:	n/a
47	chr15:43893898-43893948	HepG2	liver:	n/a
48	chr15:43879335-43879385	NHBE	bronchial:	n/a
49	chr15:43891480-43891530	PrEC	prostate:	n/a
50	chr15:43937339-43937389	NB4	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr15:43822573..43824658-chr15:43837005..43839748,2	K562	blood:
2	15:43889977-43895899..15:44001645-44015047	GM12878	blood:
3	15:43924442-43930824..15:44001645-44015047	GM12878	blood:
4	chr15:43814141..43815931-chr15:43837910..43839648,2	K562	blood:
5	15:43792489-43802874..15:43916541-43924442	Hela-S3	cervix:
6	15:43782117-43785993..15:43931042-43936532	GM12878	blood:
7	15:43916541-43924442..15:44034348-44042259	K562	blood:
8	15:43916541-43924442..15:44080886-44089111	GM12878	blood:

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

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

Extended variants
information (count: 2396 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:2396 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2251844	chr15:43836478-43836479	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs543892287	chr15:43836489-43836490	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs544409569	chr15:43836571-43836572	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs377100332	chr15:43836661-43836662	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs574054412	chr15:43836681-43836682	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs542787982	chr15:43836682-43836683	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs559689466	chr15:43836756-43836757	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs374307353	chr15:43836758-43836759	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs545248711	chr15:43836795-43836796	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs189424509	chr15:43836829-43836830	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs574495018	chr15:43836851-43836852	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs181123771	chr15:43836918-43836919	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs574475547	chr15:43836945-43836946	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs486301	chr15:43836949-43836950	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs36027289	chr15:43836983-43836984	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs487282	chr15:43837072-43837073	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551132563	chr15:43837075-43837076	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185613854	chr15:43837100-43837101	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs529790371	chr15:43837104-43837105	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546427958	chr15:43837110-43837111	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566430399	chr15:43837112-43837113	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188128355	chr15:43837114-43837115	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs113132512	chr15:43837139-43837140	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558855153	chr15:43837158-43837159	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181024774	chr15:43837159-43837160	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs71476495	chr15:43837161-43837162	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537777171	chr15:43837169-43837170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554730546	chr15:43837208-43837209	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574586256	chr15:43837212-43837213	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536747541	chr15:43837249-43837250	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2439834	chr15:43837283-43837284	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs572859294	chr15:43837304-43837305	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575725843	chr15:43837354-43837355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564966855	chr15:43837370-43837371	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2584708	chr15:43837373-43837374	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531234375	chr15:43837378-43837379	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs568027267	chr15:43837382-43837383	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs60345631	chr15:43837393-43837394	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575516432	chr15:43837401-43837402	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544619252	chr15:43837408-43837409	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372943023	chr15:43837522-43837523	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561531838	chr15:43837533-43837534	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs377148959	chr15:43837635-43837636	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs79817565	chr15:43837674-43837675	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs56710390	chr15:43837692-43837693	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530237853	chr15:43837737-43837738	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546636997	chr15:43837746-43837747	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs139954055	chr15:43837778-43837779	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545958085	chr15:43837825-43837826	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145393909	chr15:43837883-43837884	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:444 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43812000-43844400	Weak transcription	Fetal Brain Male	brain
2	chr15:43815800-43839400	Weak transcription	Stomach Mucosa	stomach
3	chr15:43818000-43852600	Weak transcription	Rectal Smooth Muscle	rectum
4	chr15:43818200-43851600	Weak transcription	Primary hematopoietic stem cells	blood
5	chr15:43822800-43842800	Weak transcription	HSMM	muscle
6	chr15:43823600-43837400	Weak transcription	Fetal Lung	lung
7	chr15:43823600-43840000	Weak transcription	Psoas Muscle	Psoas
8	chr15:43823800-43852600	Weak transcription	Primary monocytes fromperipheralblood	blood
9	chr15:43824200-43842800	Weak transcription	HSMMtube	muscle
10	chr15:43824200-43845000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr15:43824800-43853000	Weak transcription	GM12878-XiMat	blood
12	chr15:43824800-43853200	Weak transcription	Hela-S3	cervix
13	chr15:43827200-43849800	Weak transcription	Colonic Mucosa	Colon
14	chr15:43827400-43839800	Weak transcription	Colon Smooth Muscle	Colon
15	chr15:43827400-43841400	Weak transcription	NHEK	skin
16	chr15:43827400-43842400	Weak transcription	Osteobl	bone
17	chr15:43827400-43852600	Weak transcription	Left Ventricle	heart
18	chr15:43827400-43854000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr15:43827600-43837000	Weak transcription	Gastric	stomach
20	chr15:43827600-43839200	Weak transcription	Primary T cells from cord blood	blood
21	chr15:43827600-43839200	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr15:43827600-43840400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr15:43827600-43840400	Weak transcription	Fetal Stomach	stomach
24	chr15:43827600-43846800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr15:43827600-43848400	Weak transcription	Primary T helper cells fromperipheralblood	blood
26	chr15:43827600-43848600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr15:43827600-43849000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr15:43827600-43849400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr15:43827600-43851200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr15:43827600-43851400	Weak transcription	Right Ventricle	heart
31	chr15:43827600-43851800	Weak transcription	Primary B cells from peripheral blood	blood
32	chr15:43827600-43852800	Weak transcription	Lung	lung
33	chr15:43827600-43854000	Weak transcription	Aorta	Aorta
34	chr15:43827600-43855400	Weak transcription	Ovary	ovary
35	chr15:43827800-43838600	Weak transcription	Duodenum Mucosa	Duodenum
36	chr15:43827800-43839800	Weak transcription	Brain Anterior Caudate	brain
37	chr15:43827800-43839800	Weak transcription	Brain Hippocampus Middle	brain
38	chr15:43827800-43839800	Weak transcription	HMEC	breast
39	chr15:43827800-43841000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr15:43827800-43841400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr15:43827800-43842800	Weak transcription	Brain Angular Gyrus	brain
42	chr15:43827800-43845200	Weak transcription	Liver	Liver
43	chr15:43827800-43845400	Weak transcription	Stomach Smooth Muscle	stomach
44	chr15:43827800-43848200	Weak transcription	Brain Germinal Matrix	brain
45	chr15:43827800-43848600	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr15:43827800-43848800	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr15:43827800-43849600	Weak transcription	Spleen	Spleen
48	chr15:43827800-43850000	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr15:43827800-43850400	Weak transcription	Primary B cells from cord blood	blood
50	chr15:43827800-43850800	Weak transcription	Esophagus	oesophagus

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