Variant report

Variant	nsv1038660
Chromosome Location	chr15:54756184-55039913
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:805)
CpG islands
(count:61)
Chromatin interactive
region (count:17)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:805 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:54909959-54910868	HepG2	liver:	n/a	n/a
2	ATF1	chr15:54833683-54833883	K562	blood:	n/a	n/a
3	ATF2	chr15:54874932-54875503	GM12878	blood:	n/a	n/a
4	ATF2	chr15:54874932-54875387	GM12878	blood:	n/a	n/a
5	ATF2	chr15:54807907-54808243	GM12878	blood:	n/a	n/a
6	BATF	chr15:54875043-54875462	GM12878	blood:	n/a	n/a
7	BATF	chr15:54875811-54876146	GM12878	blood:	n/a	n/a
8	BATF	chr15:54807862-54808188	GM12878	blood:	n/a	chr15:54808047-54808057
9	BATF	chr15:54807870-54808716	GM12878	blood:	n/a	chr15:54808047-54808057
10	BATF	chr15:54797021-54797226	GM12878	blood:	n/a	n/a
11	BATF	chr15:54810388-54810687	GM12878	blood:	n/a	chr15:54810577-54810588
12	BATF	chr15:54908894-54909106	GM12878	blood:	n/a	chr15:54909011-54909022
13	BATF	chr15:54811859-54812097	GM12878	blood:	n/a	n/a
14	BATF	chr15:54868799-54869119	GM12878	blood:	n/a	chr15:54868969-54868980
15	BCL11A	chr15:54807818-54808188	GM12878	blood:	n/a	n/a
16	BCL11A	chr15:54807898-54808160	GM12878	blood:	n/a	n/a
17	BCL11A	chr15:54808259-54808523	GM12878	blood:	n/a	n/a
18	BCL11A	chr15:54810384-54810625	GM12878	blood:	n/a	n/a
19	BCL11A	chr15:54810414-54810654	GM12878	blood:	n/a	n/a
20	BCL11A	chr15:54875088-54875445	GM12878	blood:	n/a	n/a
21	BCL11A	chr15:54875821-54876150	GM12878	blood:	n/a	n/a
22	BCL11A	chr15:54874932-54875462	GM12878	blood:	n/a	n/a
23	BCL11A	chr15:54875822-54876112	GM12878	blood:	n/a	n/a
24	BCL11A	chr15:54808205-54808662	GM12878	blood:	n/a	n/a
25	BCL3	chr15:54807857-54808211	GM12878	blood:	n/a	n/a
26	BCLAF1	chr15:54875022-54875350	GM12878	blood:	n/a	n/a
27	BHLHE40	chr15:54874807-54876267	GM12878	blood:	n/a	n/a
28	BHLHE40	chr15:54913156-54913250	GM12878	blood:	n/a	n/a
29	BHLHE40	chr15:54811431-54812140	GM12878	blood:	n/a	n/a
30	BHLHE40	chr15:54973796-54974106	GM12878	blood:	n/a	n/a
31	BHLHE40	chr15:54807827-54808695	GM12878	blood:	n/a	n/a
32	BHLHE40	chr15:54868960-54869025	GM12878	blood:	n/a	n/a
33	BHLHE40	chr15:54909020-54909028	GM12878	blood:	n/a	n/a
34	BHLHE40	chr15:54876018-54876211	K562	blood:	n/a	n/a
35	BHLHE40	chr15:54809640-54810876	GM12878	blood:	n/a	n/a
36	BRCA1	chr15:54877809-54877948	GM12878	blood:	n/a	n/a
37	CEBPB	chr15:55021877-55021993	A549	lung:	n/a	chr15:55021919-55021930
38	CEBPB	chr15:55014411-55014566	K562	blood:	n/a	chr15:55014499-55014510
39	CEBPB	chr15:54933930-54934219	A549	lung:	n/a	chr15:54934095-54934106
40	CEBPB	chr15:54841884-54842166	HepG2	liver:	n/a	chr15:54842008-54842019 chr15:54842006-54842017 chr15:54842006-54842019
41	CEBPB	chr15:54910450-54910580	HepG2	liver:	n/a	n/a
42	CEBPB	chr15:54823919-54823990	K562	blood:	n/a	chr15:54823943-54823954
43	CEBPB	chr15:55001246-55001467	HepG2	liver:	n/a	chr15:55001370-55001381
44	CEBPB	chr15:55004347-55004481	A549	lung:	n/a	chr15:55004423-55004434
45	CEBPB	chr15:55014407-55014631	HepG2	liver:	n/a	chr15:55014499-55014510
46	CEBPB	chr15:54784805-54785027	K562	blood:	n/a	chr15:54784869-54784880
47	CEBPB	chr15:54823786-54824113	HepG2	liver:	n/a	chr15:54823943-54823954
48	CEBPB	chr15:55014370-55014653	A549	lung:	n/a	chr15:55014499-55014510
49	CEBPB	chr15:55014331-55014651	IMR90	lung:	n/a	chr15:55014499-55014510
50	CEBPB	chr15:54910340-54910679	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:54897418-54897468	HAEpiC	amniotic membrane:	n/a
2	chr15:54897418-54897468	SKMC	muscle:	n/a
3	chr15:54897418-54897468	HEK293	kidney:	embryo
4	chr15:54897418-54897468	Hela-S3	cervix:	n/a
5	chr15:54897418-54897468	GM12892	blood:	n/a
6	chr15:54897418-54897468	IMR90	lung:	fetal
7	chr15:54897418-54897468	HMEC	breast:	n/a
8	chr15:54897418-54897468	GM12891	blood:	n/a
9	chr15:54897418-54897468	AG04449	skin:	fetal
10	chr15:54897418-54897468	MCF10A-Er-Src	breast:	n/a
11	chr15:54897418-54897468	Caco-2	colon:	n/a
12	chr15:54897418-54897468	PFSK-1	brain:	n/a
13	chr15:54897418-54897468	HRCEpiC	kidney:	n/a
14	chr15:54897418-54897468	HRPEpiC	eye:	n/a
15	chr15:54897418-54897468	BE2_C	brain:	n/a
16	chr15:54897418-54897468	CMK	blood:	n/a
17	chr15:54897418-54897468	SK-N-MC	brain:	n/a
18	chr15:54897418-54897468	NHBE	bronchial:	n/a
19	chr15:54897418-54897468	HNPCEpiC	eye:	n/a
20	chr15:54897418-54897468	PANC-1	pancreas:	n/a
21	chr15:54897418-54897468	NT2-D1	testis:	n/a
22	chr15:54897418-54897468	RPTEC	kidney:	n/a
23	chr15:54897418-54897468	HCPEpiC	choroid plexus:	n/a
24	chr15:54897418-54897468	ECC-1	luminal epithelium:	n/a
25	chr15:54897418-54897468	NH-A	brain:	n/a
26	chr15:54897418-54897468	BJ	skin:	n/a
27	chr15:54897418-54897468	HEEpiC	esophagus:	n/a
28	chr15:54897418-54897468	T-47D	breast:	n/a
29	chr15:54897418-54897468	GM06990	blood:	n/a
30	chr15:54897418-54897468	Hepatocyte	liver:	n/a
31	chr15:54897418-54897468	K562	blood:	n/a
32	chr15:54897418-54897468	SAEC	small airway:	n/a
33	chr15:54897418-54897468	AoSMC	blood vessel:	n/a
34	chr15:54897418-54897468	HCF	heart:	n/a
35	chr15:54897418-54897468	Jurkat	blood:	n/a
36	chr15:54897418-54897468	LNCaP	prostate:	n/a
37	chr15:54897418-54897468	GM12878	blood:	n/a
38	chr15:54897418-54897468	AG09319	gingival:	n/a
39	chr15:54897418-54897468	HRE	kidney:	n/a
40	chr15:54897418-54897468	NHDF-neo	bronchial:	n/a
41	chr15:54897418-54897468	AG09309	skin:	n/a
42	chr15:54897418-54897468	ProgFib	skin:	n/a
43	chr15:54897418-54897468	A549	lung:	n/a
44	chr15:54897418-54897468	MCF-7	breast:	n/a
45	chr15:54897418-54897468	H1-hESC	embryonic stem cell:	embryo
46	chr15:54897418-54897468	SK-N-SH	brain:	n/a
47	chr15:54897418-54897468	NB4	blood:	n/a
48	chr15:54897418-54897468	AG10803	skin:	n/a
49	chr15:54897418-54897468	HepG2	liver:	n/a
50	chr15:54897418-54897468	HPAEpiC	pulmonary alveolar:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:54860759..54864506-chr15:54869181..54871283,4	K562	blood:
2	chr15:54860759..54863640-chr15:54869706..54871283,2	K562	blood:
3	chr15:54860759..54863640-chr15:54869706..54871283,2	K562	blood:
4	chr15:54910155..54912492-chr15:54912771..54915484,2	MCF-7	breast:
5	chr15:54910155..54912492-chr15:54912771..54915484,2	MCF-7	breast:
6	chr15:54867084..54868948-chr15:54872476..54874542,2	K562	blood:
7	chr15:55000191..55003653-chr15:55007581..55011163,3	MCF-7	breast:
8	chr15:54867084..54868948-chr15:54872476..54874542,2	K562	blood:
9	chr15:55000280..55003286-chr15:55005591..55008128,3	K562	blood:
10	chr15:54926871..54929608-chr15:54933305..54935449,2	K562	blood:
11	chr15:54812666..54814961-chr15:54822160..54825055,2	MCF-7	breast:
12	chr15:54812666..54814961-chr15:54822160..54825055,2	MCF-7	breast:
13	chr15:54926871..54929608-chr15:54933305..54935449,2	K562	blood:
14	chr15:55000280..55003286-chr15:55005591..55008128,3	K562	blood:
15	chr15:54860759..54864506-chr15:54869181..54871283,4	K562	blood:
16	chr15:55000191..55003653-chr15:55007581..55011163,3	MCF-7	breast:
17	chr15:54777517..54778098-chr15:55488919..55489423,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RSL24D1-4	chr15:54902051-54903329	NONHSAT043976

No data

(count:2 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	UNC13C	hsa-miR-128-3p	chr15:54919879-54919886
2	UNC13C	hsa-miR-128-3p	chr15:54919866-54919886

Variant related genes	Relation type
UNC13C	TF binding region
UNC13C	CpG island
ENSG00000137876	chromatin interactions

Extended variants
information (count: 7569 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:7569 , 50 per page) page: 1 2 3 4 5 6 7 ... 152

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11633610	chr15:54756184-54756185	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs368510142	chr15:54756223-54756224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552587320	chr15:54756242-54756243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs565630862	chr15:54756288-54756289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs534660001	chr15:54756374-54756375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554530140	chr15:54756400-54756401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551352878	chr15:54756433-54756434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574383996	chr15:54756445-54756446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs371549780	chr15:54756464-54756465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs182713682	chr15:54756473-54756474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs187535416	chr15:54756480-54756481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192792915	chr15:54756484-54756485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531859166	chr15:54756514-54756515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs147890950	chr15:54756536-54756537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528760761	chr15:54756539-54756540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542192450	chr15:54756574-54756575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs4776231	chr15:54756628-54756629	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs530830203	chr15:54756629-54756630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs535303246	chr15:54756639-54756640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183844212	chr15:54756663-54756664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549903305	chr15:54756781-54756782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs368303497	chr15:54756801-54756802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187898373	chr15:54756802-54756803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191981970	chr15:54756815-54756816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551951577	chr15:54756818-54756819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565767456	chr15:54756832-54756833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547204590	chr15:54756841-54756842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs568536764	chr15:54756848-54756849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554584133	chr15:54756861-54756862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568020098	chr15:54756896-54756897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145330450	chr15:54756904-54756905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557055118	chr15:54756940-54756941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs184593916	chr15:54756963-54756964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs79680601	chr15:54757002-54757003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553587921	chr15:54757025-54757026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs573371770	chr15:54757063-54757064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs542478127	chr15:54757070-54757071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs116742812	chr15:54757107-54757108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs74016625	chr15:54757116-54757117	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs544193041	chr15:54757117-54757118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564189980	chr15:54757122-54757123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575217763	chr15:54757130-54757131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs145124734	chr15:54757135-54757136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149105606	chr15:54757155-54757156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113281032	chr15:54757156-54757157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559465358	chr15:54757184-54757185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528297224	chr15:54757196-54757197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs12439419	chr15:54767612-54767613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563673087	chr15:54767621-54767622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs202033383	chr15:54767637-54767638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Urothelial carcinoma	21177765	CNVD
Pancreatic cancer	17952125	CNVD
Renal cell carcinoma	21215367	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	17440070	CNVD
Cancer	20164919	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:341 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:54754200-54757200	Weak transcription	Fetal Lung	lung
2	chr15:54767600-54767800	Weak transcription	Aorta	Aorta
3	chr15:54769200-54777600	Weak transcription	Aorta	Aorta
4	chr15:54773400-54774200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr15:54774200-54775000	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr15:54774400-54774800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr15:54774400-54775000	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr15:54774600-54775000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr15:54774600-54775000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr15:54775200-54794000	Weak transcription	Fetal Lung	lung
11	chr15:54777600-54777800	ZNF genes & repeats	Aorta	Aorta
12	chr15:54777800-54810400	Weak transcription	Aorta	Aorta
13	chr15:54784800-54785000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr15:54784800-54785200	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr15:54785000-54785600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr15:54785200-54785400	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr15:54785200-54791000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr15:54785400-54786800	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr15:54785600-54791200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr15:54786800-54787200	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr15:54786800-54787200	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr15:54786800-54787400	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr15:54787000-54787400	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr15:54787000-54791200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr15:54787200-54790800	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr15:54787200-54791000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr15:54787400-54790800	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr15:54787400-54791000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr15:54789400-54789800	Enhancers	H9 Cell Line	embryonic stem cell
30	chr15:54789800-54791400	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr15:54790800-54793200	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr15:54790800-54793200	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr15:54791000-54792600	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr15:54791000-54793000	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr15:54791000-54793200	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr15:54791000-54793200	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr15:54791200-54792800	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr15:54791200-54792800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr15:54791400-54792400	Enhancers	H9 Cell Line	embryonic stem cell
40	chr15:54791600-54792400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr15:54792200-54792800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr15:54792400-54792800	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr15:54792800-54793200	Enhancers	H9 Cell Line	embryonic stem cell
44	chr15:54794000-54795400	Enhancers	Fetal Lung	lung
45	chr15:54795400-54799400	Weak transcription	Fetal Lung	lung
46	chr15:54798200-54799000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr15:54799000-54799800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr15:54799000-54799800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr15:54799000-54802000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr15:54799400-54799800	Enhancers	Primary hematopoietic stem cells short term culture	blood

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