Variant report

Variant	nsv946078
Chromosome Location	chr1:93302864-93303580
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:62)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr1:93302949-93303162	T-47D	breast:	n/a	n/a
2	HEY1	chr1:93302944-93303248	K562	blood:	n/a	n/a
3	HEY1	chr1:93302501-93303186	HepG2	liver:	n/a	n/a
4	HEY1	chr1:93303463-93303812	K562	blood:	n/a	n/a
5	NFATC1	chr1:93303382-93304187	GM12878	blood:	n/a	n/a
6	POLR2A	chr1:93301185-93302961	K562	blood:	n/a	n/a
7	POLR2A	chr1:93303001-93304270	HepG2	liver:	n/a	n/a
8	POLR2A	chr1:93302415-93302895	H1-hESC	embryonic stem cell:	n/a	n/a
9	POLR2A	chr1:93302585-93302970	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr1:93303274-93305956	Hela-S3	cervix:	n/a	n/a
11	POLR2A	chr1:93302966-93303319	MCF-7	breast:	n/a	n/a
12	POLR2A	chr1:93302678-93302964	H1-hESC	embryonic stem cell:	n/a	n/a
13	POLR2A	chr1:93303378-93303844	PFSK-1	brain:	n/a	n/a
14	POLR2A	chr1:93303257-93303724	GM12891	blood:	n/a	n/a
15	POLR2A	chr1:93301952-93304401	GM12891	blood:	n/a	n/a
16	POLR2A	chr1:93302901-93302960	MCF-7	breast:	n/a	n/a
17	POLR2A	chr1:93301994-93304325	GM12878	blood:	n/a	n/a
18	POLR2A	chr1:93302920-93302940	Hela-S3	cervix:	n/a	n/a
19	POLR2A	chr1:93303166-93307156	K562	blood:	n/a	n/a
20	POLR2A	chr1:93302823-93302941	HepG2	liver:	n/a	n/a
21	POLR2A	chr1:93303363-93304272	K562	blood:	n/a	n/a
22	POLR2A	chr1:93301402-93304643	PFSK-1	brain:	n/a	n/a
23	POLR2A	chr1:93301566-93303131	PFSK-1	brain:	n/a	n/a
24	POLR2A	chr1:93302527-93303176	SK-N-MC	brain:	n/a	n/a
25	POLR2A	chr1:93303370-93303855	GM12892	blood:	n/a	n/a
26	POLR2A	chr1:93301579-93302952	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr1:93302382-93303875	GM12878	blood:	n/a	n/a
28	POLR2A	chr1:93303250-93303302	MCF10A-Er-Src	breast:	n/a	n/a
29	POLR2A	chr1:93302966-93303919	GM12892	blood:	n/a	n/a
30	POLR2A	chr1:93303312-93303703	SK-N-SH	brain:	n/a	n/a
31	POLR2A	chr1:93301157-93303829	GM12878	blood:	n/a	n/a
32	POLR2A	chr1:93303382-93303823	K562	blood:	n/a	n/a
33	POLR2A	chr1:93302532-93302966	HL-60	blood:	n/a	n/a
34	POLR2A	chr1:93303462-93303771	K562	blood:	n/a	n/a
35	POLR2A	chr1:93302546-93302881	Hela-S3	cervix:	n/a	n/a
36	POLR2A	chr1:93303476-93303729	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr1:93301817-93304585	HepG2	liver:	n/a	n/a
38	POLR2A	chr1:93303468-93303864	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr1:93303264-93304423	SK-N-MC	brain:	n/a	n/a
40	POLR2A	chr1:93302952-93303216	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr1:93301434-93307185	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr1:93302907-93302954	HepG2	liver:	n/a	n/a
43	POLR2A	chr1:93302740-93302945	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr1:93302359-93302939	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr1:93301216-93310285	K562	blood:	n/a	n/a
46	POLR2A	chr1:93302871-93302892	MCF-7	breast:	n/a	n/a
47	POLR2A	chr1:93303221-93303789	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr1:93303348-93304208	A549	lung:	n/a	n/a
49	POLR2A	chr1:93302440-93303763	GM12892	blood:	n/a	n/a
50	POLR2A	chr1:93303005-93303189	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:93302925-93302975	HRPEpiC	eye:	n/a
2	chr1:93302925-93302975	SKMC	muscle:	n/a
3	chr1:93302925-93302975	HAEpiC	amniotic membrane:	n/a
4	chr1:93302925-93302975	HUVEC	blood vessel:	n/a
5	chr1:93302925-93302975	RPTEC	kidney:	n/a
6	chr1:93302925-93302975	GM12892	blood:	n/a
7	chr1:93302925-93302975	HIPEpiC	eye:	n/a
8	chr1:93302925-93302975	SK-N-SH_RA	brain:	n/a
9	chr1:93302925-93302975	ProgFib	skin:	n/a
10	chr1:93302925-93302975	HCT-116	colon:	n/a
11	chr1:93302925-93302975	SAEC	small airway:	n/a
12	chr1:93302925-93302975	NHBE	bronchial:	n/a
13	chr1:93302925-93302975	HMEC	breast:	n/a
14	chr1:93302925-93302975	MCF10A-Er-Src	breast:	n/a
15	chr1:93302925-93302975	ovcar-3	ovarian:	n/a
16	chr1:93302925-93302975	H1-hESC	embryonic stem cell:	embryo
17	chr1:93302925-93302975	BE2_C	brain:	n/a
18	chr1:93302925-93302975	Hepatocyte	liver:	n/a
19	chr1:93302925-93302975	PFSK-1	brain:	n/a
20	chr1:93302925-93302975	HRCEpiC	kidney:	n/a
21	chr1:93302925-93302975	Jurkat	blood:	n/a
22	chr1:93302925-93302975	AG10803	skin:	n/a
23	chr1:93302925-93302975	T-47D	breast:	n/a
24	chr1:93302925-93302975	HCF	heart:	n/a
25	chr1:93302925-93302975	AoSMC	blood vessel:	n/a
26	chr1:93302925-93302975	HepG2	liver:	n/a
27	chr1:93302925-93302975	HRE	kidney:	n/a
28	chr1:93302925-93302975	SK-N-MC	brain:	n/a
29	chr1:93302925-93302975	U87	brain:	n/a
30	chr1:93302925-93302975	IMR90	lung:	fetal
31	chr1:93302925-93302975	AG09319	gingival:	n/a
32	chr1:93302925-93302975	NB4	blood:	n/a
33	chr1:93302925-93302975	HNPCEpiC	eye:	n/a
34	chr1:93302925-93302975	K562	blood:	n/a
35	chr1:93302925-93302975	HL-60	blood:	n/a
36	chr1:93302925-93302975	AG04449	skin:	fetal
37	chr1:93302925-93302975	GM19239	blood:	n/a
38	chr1:93302925-93302975	PrEC	prostate:	n/a
39	chr1:93302925-93302975	HCPEpiC	choroid plexus:	n/a
40	chr1:93302925-93302975	GM12891	blood:	n/a
41	chr1:93302925-93302975	HPAEpiC	pulmonary alveolar:	n/a
42	chr1:93302925-93302975	NT2-D1	testis:	n/a
43	chr1:93302925-93302975	GM12878	blood:	n/a
44	chr1:93302925-93302975	Caco-2	colon:	n/a
45	chr1:93302925-93302975	LNCaP	prostate:	n/a
46	chr1:93302925-93302975	HEEpiC	esophagus:	n/a
47	chr1:93302925-93302975	NH-A	brain:	n/a
48	chr1:93302925-93302975	A549	lung:	n/a
49	chr1:93302925-93302975	BJ	skin:	n/a
50	chr1:93302925-93302975	ECC-1	luminal epithelium:	n/a

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No.	Distal block	Cell Line	Cell type
1	chr1:93214862..93218519-chr1:93302722..93305780,4	K562	blood:
2	chr1:93303345..93305385-chr1:93311213..93313203,2	MCF-7	breast:
3	chr1:93302921..93305469-chr1:93643662..93645581,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RPL5	hsa-miR-328-3p	chr1:93303070-93303091

Variant related genes	Relation type
ENSG00000251795	TF binding region
SNORA66	TF binding region
ENSG00000251795	CpG island
SNORA66	CpG island
ENSG00000234202	chromatin interactions
ENSG00000207022	chromatin interactions
ENSG00000122483	chromatin interactions

Extended variants
information (count: 27 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368454833	chr1:93302900-93302901	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs371558666	chr1:93302904-93302905	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs374993851	chr1:93302908-93302909	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs77093817	chr1:93302919-93302920	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs367590103	chr1:93302925-93302926	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs371345041	chr1:93302949-93302950	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs546946459	chr1:93302983-93302984	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs369811492	chr1:93302984-93302985	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs375148060	chr1:93303001-93303002	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs528939210	chr1:93303071-93303072	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region miRNA target site	5 gene(s)	Overlapped CNVs	n/a
11	rs11540832	chr1:93303114-93303115	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs568863745	chr1:93303176-93303177	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs576330538	chr1:93303186-93303187	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs200087538	chr1:93303188-93303189	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs370085772	chr1:93303207-93303208	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs3831193	chr1:93303227-93303228	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs398074158	chr1:93303228-93303229	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs552513062	chr1:93303234-93303235	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs571059513	chr1:93303244-93303245	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs549274227	chr1:93303285-93303286	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs534885982	chr1:93303411-93303412	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs562730320	chr1:93303419-93303420	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs6659942	chr1:93303451-93303452	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs141502873	chr1:93303467-93303468	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs143761019	chr1:93303478-93303479	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs575663711	chr1:93303497-93303498	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs150488958	chr1:93303521-93303522	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	16397240	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Prostate cancer	19156837	CNVD
Autism	17483303	CNVD
Malignant melanoma	17260012	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:146 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:93299200-93303800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr1:93299200-93305400	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
3	chr1:93299200-93306200	Genic enhancers	Primary T helper memory cells from peripheral blood 1	blood
4	chr1:93299200-93310400	Strong transcription	Fetal Muscle Trunk	muscle
5	chr1:93299400-93307200	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr1:93299400-93309200	Strong transcription	Placenta Amnion	Placenta Amnion
7	chr1:93299600-93303400	Genic enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr1:93299600-93304400	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chr1:93299600-93306000	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr1:93299600-93306600	Genic enhancers	Primary T killer memory cells from peripheral blood	blood
11	chr1:93299600-93309000	Weak transcription	Esophagus	oesophagus
12	chr1:93299600-93309800	Strong transcription	Primary neutrophils fromperipheralblood	blood
13	chr1:93299600-93310000	Strong transcription	Placenta	Placenta
14	chr1:93299600-93310400	Strong transcription	Fetal Thymus	thymus
15	chr1:93299800-93303600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr1:93299800-93304200	Weak transcription	Gastric	stomach
17	chr1:93299800-93304400	Genic enhancers	NHDF-Ad	bronchial
18	chr1:93299800-93310600	Strong transcription	Fetal Intestine Large	intestine
19	chr1:93299800-93311600	Strong transcription	Fetal Muscle Leg	muscle
20	chr1:93300000-93303800	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr1:93300000-93305000	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr1:93300000-93305800	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
23	chr1:93300000-93306000	Genic enhancers	Primary T cells from cord blood	blood
24	chr1:93300000-93306200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr1:93300000-93309800	Strong transcription	Thymus	Thymus
26	chr1:93300000-93310000	Strong transcription	HUES6 Cell Line	embryonic stem cell
27	chr1:93300000-93310000	Strong transcription	Monocytes-CD14+_RO01746	blood
28	chr1:93300000-93310200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr1:93300200-93303600	Weak transcription	Brain Angular Gyrus	brain
30	chr1:93300200-93305400	Genic enhancers	HepG2	liver
31	chr1:93300200-93306000	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
32	chr1:93300200-93306000	Genic enhancers	Primary T helper cells fromperipheralblood	blood
33	chr1:93300200-93306600	Strong transcription	Fetal Kidney	kidney
34	chr1:93300200-93308000	Strong transcription	Colonic Mucosa	Colon
35	chr1:93300200-93309200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr1:93300200-93310000	Strong transcription	HSMMtube	muscle
37	chr1:93300200-93310200	Strong transcription	Primary monocytes fromperipheralblood	blood
38	chr1:93300200-93310400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr1:93300400-93305000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr1:93300400-93305000	Strong transcription	Fetal Lung	lung
41	chr1:93300400-93305800	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr1:93300400-93306600	Strong transcription	Lung	lung
43	chr1:93300400-93310000	Strong transcription	Rectal Mucosa Donor 29	rectum
44	chr1:93300400-93316000	Strong transcription	Primary B cells from cord blood	blood
45	chr1:93300600-93304200	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr1:93300600-93304400	Genic enhancers	Osteobl	bone
47	chr1:93300600-93305200	Strong transcription	Brain Inferior Temporal Lobe	brain
48	chr1:93300600-93308800	Strong transcription	H9 Cell Line	embryonic stem cell
49	chr1:93300600-93309200	Strong transcription	Cortex derived primary cultured neurospheres	brain
50	chr1:93300600-93310000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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