Variant report

Variant	nsv903844
Chromosome Location	chr15:31736091-31781988
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1288)
CpG islands
(count:1346)
Chromatin interactive
region (count:30)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1288 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:31780793-31781117	K562	blood:	n/a	n/a
2	ARID3A	chr15:31780846-31781135	HepG2	liver:	n/a	n/a
3	ATF1	chr15:31736055-31736373	K562	blood:	n/a	n/a
4	ATF1	chr15:31739062-31739258	K562	blood:	n/a	n/a
5	ATF2	chr15:31780042-31780621	GM12878	blood:	n/a	n/a
6	ATF2	chr15:31751192-31751725	GM12878	blood:	n/a	n/a
7	ATF2	chr15:31751038-31751815	GM12878	blood:	n/a	n/a
8	ATF2	chr15:31735877-31736427	GM12878	blood:	n/a	n/a
9	ATF2	chr15:31780255-31781128	GM12878	blood:	n/a	n/a
10	ATF2	chr15:31735790-31736388	GM12878	blood:	n/a	n/a
11	ATF3	chr15:31736109-31736314	K562	blood:	n/a	n/a
12	BACH1	chr15:31747847-31747986	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr15:31775531-31776385	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr15:31751257-31751640	GM12878	blood:	n/a	n/a
15	BATF	chr15:31780250-31780659	GM12878	blood:	n/a	chr15:31780490-31780500
16	BATF	chr15:31735728-31736270	GM12878	blood:	n/a	chr15:31735937-31735947
17	BATF	chr15:31780127-31781131	GM12878	blood:	n/a	chr15:31780490-31780500
18	BCL11A	chr15:31780285-31780642	GM12878	blood:	n/a	n/a
19	BCL11A	chr15:31780237-31780696	GM12878	blood:	n/a	n/a
20	BCL11A	chr15:31751147-31751700	GM12878	blood:	n/a	n/a
21	BCL3	chr15:31759025-31759318	GM12878	blood:	n/a	n/a
22	BCL3	chr15:31749134-31749475	GM12878	blood:	n/a	n/a
23	BCL3	chr15:31780314-31780731	GM12878	blood:	n/a	n/a
24	BCL3	chr15:31749116-31749537	GM12878	blood:	n/a	n/a
25	BCLAF1	chr15:31751116-31751769	GM12878	blood:	n/a	n/a
26	BCLAF1	chr15:31765120-31765606	GM12878	blood:	n/a	n/a
27	BHLHE40	chr15:31735818-31736245	GM12878	blood:	n/a	n/a
28	BHLHE40	chr15:31751153-31751981	GM12878	blood:	n/a	n/a
29	BHLHE40	chr15:31765070-31765532	GM12878	blood:	n/a	n/a
30	BHLHE40	chr15:31780166-31781139	GM12878	blood:	n/a	n/a
31	BHLHE40	chr15:31740780-31741134	K562	blood:	n/a	n/a
32	BRCA1	chr15:31736086-31736359	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr15:31780865-31781329	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr15:31775170-31775650	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr15:31744226-31744567	IMR90	lung:	n/a	n/a
36	CEBPB	chr15:31736056-31736501	A549	lung:	n/a	n/a
37	CEBPB	chr15:31780797-31781118	K562	blood:	n/a	n/a
38	CEBPB	chr15:31780347-31781396	IMR90	lung:	n/a	n/a
39	CEBPB	chr15:31780796-31781145	A549	lung:	n/a	n/a
40	CEBPB	chr15:31780589-31781407	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr15:31736074-31736434	A549	lung:	n/a	n/a
42	CEBPB	chr15:31736074-31736414	K562	blood:	n/a	n/a
43	CEBPB	chr15:31764050-31764472	IMR90	lung:	n/a	n/a
44	CEBPB	chr15:31744179-31744562	A549	lung:	n/a	n/a
45	CEBPB	chr15:31744337-31744446	HepG2	liver:	n/a	n/a
46	CEBPB	chr15:31736052-31736442	IMR90	lung:	n/a	n/a
47	CEBPB	chr15:31780805-31781109	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr15:31736063-31736397	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr15:31780806-31781068	HepG2	liver:	n/a	n/a
50	CHD1	chr15:31780006-31782011	IMR90	lung:	n/a	n/a

(count:1346 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:31781955-31782005	BE2_C	brain:	n/a
2	chr15:31776741-31776791	Hepatocyte	liver:	n/a
3	chr15:31742799-31742849	LNCaP	prostate:	n/a
4	chr15:31742799-31742849	SAEC	small airway:	n/a
5	chr15:31781955-31782005	BE2_C	brain:	n/a
6	chr15:31776741-31776791	Hepatocyte	liver:	n/a
7	chr15:31742799-31742849	LNCaP	prostate:	n/a
8	chr15:31742799-31742849	SAEC	small airway:	n/a
9	chr15:31744207-31744257	H1-hESC	embryonic stem cell:	embryo
10	chr15:31746330-31746380	HCM	heart:	n/a
11	chr15:31745729-31745779	HRCEpiC	kidney:	n/a
12	chr15:31773057-31773107	AG10803	skin:	n/a
13	chr15:31776741-31776791	NHBE	bronchial:	n/a
14	chr15:31737459-31737509	AG04450	lung:	fetal
15	chr15:31764211-31764261	NH-A	brain:	n/a
16	chr15:31775049-31775099	ECC-1	luminal epithelium:	n/a
17	chr15:31749573-31749623	IMR90	lung:	fetal
18	chr15:31775049-31775099	HCF	heart:	n/a
19	chr15:31744207-31744257	HRPEpiC	eye:	n/a
20	chr15:31745916-31745966	SKMC	muscle:	n/a
21	chr15:31777358-31777408	HNPCEpiC	eye:	n/a
22	chr15:31776450-31776500	PrEC	prostate:	n/a
23	chr15:31744207-31744257	ECC-1	luminal epithelium:	n/a
24	chr15:31775406-31775456	T-47D	breast:	n/a
25	chr15:31775406-31775456	Jurkat	blood:	n/a
26	chr15:31744207-31744257	CMK	blood:	n/a
27	chr15:31775049-31775099	H1-hESC	embryonic stem cell:	embryo
28	chr15:31775406-31775456	HRCEpiC	kidney:	n/a
29	chr15:31776741-31776791	PrEC	prostate:	n/a
30	chr15:31746330-31746380	SAEC	small airway:	n/a
31	chr15:31775049-31775099	HL-60	blood:	n/a
32	chr15:31776450-31776500	AoSMC	blood vessel:	n/a
33	chr15:31742799-31742849	AG10803	skin:	n/a
34	chr15:31764211-31764261	U87	brain:	n/a
35	chr15:31737459-31737509	MCF10A-Er-Src	breast:	n/a
36	chr15:31775049-31775099	GM12892	blood:	n/a
37	chr15:31780722-31780772	T-47D	breast:	n/a
38	chr15:31777358-31777408	Jurkat	blood:	n/a
39	chr15:31777358-31777408	NB4	blood:	n/a
40	chr15:31780722-31780772	AG04449	skin:	fetal
41	chr15:31773057-31773107	HRCEpiC	kidney:	n/a
42	chr15:31776741-31776791	U87	brain:	n/a
43	chr15:31742799-31742849	HRPEpiC	eye:	n/a
44	chr15:31742799-31742849	NHBE	bronchial:	n/a
45	chr15:31775049-31775099	HCM	heart:	n/a
46	chr15:31775406-31775456	HPAEpiC	pulmonary alveolar:	n/a
47	chr15:31774773-31774823	HCM	heart:	n/a
48	chr15:31776741-31776791	NH-A	brain:	n/a
49	chr15:31780722-31780772	Hela-S3	cervix:	n/a
50	chr15:31745916-31745966	IMR90	lung:	fetal

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:31732939..31734910-chr15:31736139..31739107,2	MCF-7	breast:
2	chr15:31507301..31508500-chr15:31780431..31781449,6	K562	blood:
3	chr15:31748477..31753108-chr15:31776889..31783172,7	MCF-7	breast:
4	chr15:31753081..31754904-chr15:31769113..31772729,3	MCF-7	breast:
5	chr15:31753115..31755985-chr15:31766097..31768042,2	MCF-7	breast:
6	chr15:31728928..31731704-chr15:31776995..31778781,2	MCF-7	breast:
7	chr15:31748477..31753108-chr15:31776889..31783172,7	MCF-7	breast:
8	chr15:31775112..31777688-chr15:31780214..31782887,2	K562	blood:
9	chr15:31492529..31493483-chr15:31780441..31781476,6	MCF-7	breast:
10	chr15:31729614..31735490-chr15:31778794..31782835,6	MCF-7	breast:
11	chr15:31780894..31782465-chr15:31785232..31787543,2	MCF-7	breast:
12	chr15:31747904..31750478-chr15:31754531..31757245,2	MCF-7	breast:
13	chr15:31489768..31490355-chr15:31780489..31781405,2	K562	blood:
14	chr15:31492707..31493313-chr15:31780465..31781069,2	MCF-7	breast:
15	chr15:31768996..31771688-chr15:31773371..31775681,2	MCF-7	breast:
16	chr15:31753960..31755078-chr15:31780591..31781425,3	MCF-7	breast:
17	chr15:31775112..31777688-chr15:31780214..31782887,2	K562	blood:
18	chr15:31753960..31755078-chr15:31780591..31781425,3	MCF-7	breast:
19	chr15:31747904..31750478-chr15:31754531..31757245,2	MCF-7	breast:
20	chr15:31727262..31728165-chr15:31780632..31781327,2	MCF-7	breast:
21	chr15:31753081..31754904-chr15:31769113..31772729,3	MCF-7	breast:
22	chr15:31730666..31732248-chr15:31779741..31781482,12	MCF-7	breast:
23	chr15:31731428..31732434-chr15:31780398..31781184,5	K562	blood:
24	chr15:31731222..31732109-chr15:31780643..31781604,3	MCF-7	breast:
25	chr15:31768996..31771688-chr15:31773371..31775681,2	MCF-7	breast:
26	chr15:31753115..31755985-chr15:31766097..31768042,2	MCF-7	breast:
27	chr15:31723431..31726207-chr15:31734992..31737659,2	K562	blood:
28	chr15:31492924..31493816-chr15:31781800..31782800,3	K562	blood:
29	chr15:31507689..31508257-chr15:31779754..31780346,2	K562	blood:
30	chr15:31731861..31735385-chr15:31748681..31751856,6	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OTUD7A-1	chr15:31767607-31770705	NONHSAT041463

No data

Variant related genes	Relation type
ENSG00000259696	TF binding region
ENSG00000259696	CpG island
ENSG00000259448	chromatin interactions

Extended variants
information (count: 1939 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1939 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4779527	chr15:31736091-31736092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs200197099	chr15:31736130-31736131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs553834069	chr15:31736132-31736133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs567257494	chr15:31736162-31736163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs536396139	chr15:31736181-31736182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs191022287	chr15:31736227-31736228	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs16956738	chr15:31736231-31736232	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs544803329	chr15:31736257-31736258	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs8042575	chr15:31736355-31736356	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs578216697	chr15:31736360-31736361	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs77275339	chr15:31736402-31736403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs560154660	chr15:31736433-31736434	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs114031860	chr15:31736441-31736442	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs532405759	chr15:31736448-31736449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs10640799	chr15:31736455-31736456	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs35823872	chr15:31736456-31736457	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs3223246	chr15:31736457-31736458	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs547826096	chr15:31736478-31736479	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs56825433	chr15:31736479-31736480	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs57116254	chr15:31736480-31736481	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs563009666	chr15:31736490-31736491	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531679470	chr15:31736642-31736643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs114597488	chr15:31736678-31736679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs536773437	chr15:31736689-31736690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs527621370	chr15:31736697-31736698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs185946861	chr15:31736700-31736701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs534902190	chr15:31736715-31736716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567517150	chr15:31736720-31736721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs191281780	chr15:31736729-31736730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs4779877	chr15:31736764-31736765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs148482383	chr15:31736803-31736804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs538331487	chr15:31736813-31736814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs143597615	chr15:31736819-31736820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs537649222	chr15:31736820-31736821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs377634304	chr15:31736828-31736829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs147196373	chr15:31736851-31736852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs183048039	chr15:31736859-31736860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs558003576	chr15:31736862-31736863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs554047131	chr15:31736868-31736869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs371300113	chr15:31736875-31736876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs374353253	chr15:31736876-31736877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs187693376	chr15:31736886-31736887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs192304913	chr15:31736896-31736897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528530201	chr15:31736902-31736903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs576511442	chr15:31736944-31736945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs182451864	chr15:31736945-31736946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs565131587	chr15:31736979-31736980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs56411443	chr15:31736994-31736995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs140539798	chr15:31737001-31737002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs187844382	chr15:31737007-31737008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	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
Hodgkin''s lymphoma	18641027	CNVD
Melanoma	18172304	CNVD
Autism	17322880	CNVD
Prader-willi syndrome	19329560	CNVD
Autism	17999366	CNVD
Autism	17901113	CNVD
Neurodevelopmental disorder	17015230	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	18923513	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
Gastrointestinal stromal cancer	20818650	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	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
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Epilepsy	20502679	CNVD
small cell lung cancer	20016488	CNVD
Autism	19521722	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Autism	19050728	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Schizophrenia	19443537	CNVD
Epilepsy	20923578	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Olfactory neuroblastoma	18408657	CNVD
Pancreatic cancer	17952125	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD

Chromatin state (count:1243 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31732800-31737400	Enhancers	NHDF-Ad	bronchial
2	chr15:31733400-31736600	Enhancers	NHLF	lung
3	chr15:31733400-31741000	Weak transcription	Spleen	Spleen
4	chr15:31733600-31736200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr15:31733600-31736200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr15:31733600-31736400	Enhancers	HUVEC	blood vessel
7	chr15:31733600-31736600	Enhancers	Muscle Satellite Cultured Cells	--
8	chr15:31733600-31736800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr15:31733600-31738000	Enhancers	GM12878-XiMat	blood
10	chr15:31733800-31736400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr15:31733800-31736400	Enhancers	HSMM	muscle
12	chr15:31733800-31736400	Enhancers	NH-A	brain
13	chr15:31733800-31736600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr15:31733800-31737000	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr15:31733800-31741800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr15:31734200-31736400	Enhancers	HMEC	breast
17	chr15:31734200-31740400	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr15:31734200-31740800	Weak transcription	Placenta	Placenta
19	chr15:31734200-31740800	Weak transcription	Stomach Mucosa	stomach
20	chr15:31734400-31736600	Enhancers	Hela-S3	cervix
21	chr15:31734400-31740200	Weak transcription	Esophagus	oesophagus
22	chr15:31734400-31740600	Weak transcription	Adipose Nuclei	Adipose
23	chr15:31734400-31740800	Weak transcription	Fetal Thymus	thymus
24	chr15:31734400-31750000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr15:31734600-31736200	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr15:31734600-31736400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr15:31734600-31737000	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr15:31734600-31740600	Weak transcription	Primary T cells from cord blood	blood
29	chr15:31734600-31741200	Weak transcription	Gastric	stomach
30	chr15:31734800-31736600	Enhancers	A549	lung
31	chr15:31735000-31736200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr15:31735000-31736200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr15:31735200-31736200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr15:31735200-31736600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr15:31735200-31736600	Enhancers	Osteobl	bone
36	chr15:31735400-31736400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr15:31735400-31736600	Enhancers	NHEK	skin
38	chr15:31735400-31740600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr15:31735400-31741000	Weak transcription	HSMMtube	muscle
40	chr15:31735600-31736400	Enhancers	Primary B cells from peripheral blood	blood
41	chr15:31735600-31736600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr15:31735600-31736600	Enhancers	Small Intestine	intestine
43	chr15:31735600-31736800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
44	chr15:31735800-31736400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr15:31735800-31736400	Enhancers	Primary hematopoietic stem cells	blood
46	chr15:31735800-31736400	Enhancers	Sigmoid Colon	Sigmoid Colon
47	chr15:31735800-31736600	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr15:31735800-31736600	Enhancers	Duodenum Mucosa	Duodenum
49	chr15:31735800-31736800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr15:31736000-31736200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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