Variant report

Variant	nsv889397
Chromosome Location	chr7:147471710-147585819
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:314)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:314 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:147573807-147573905	K562	blood:	n/a	n/a
2	ATF1	chr7:147528563-147528613	K562	blood:	n/a	n/a
3	CCNT2	chr7:147506163-147506338	K562	blood:	n/a	n/a
4	CCNT2	chr7:147489824-147489960	K562	blood:	n/a	n/a
5	CEBPB	chr7:147571723-147571943	A549	lung:	n/a	n/a
6	CEBPB	chr7:147489290-147489429	K562	blood:	n/a	n/a
7	CEBPB	chr7:147555793-147555840	HepG2	liver:	n/a	n/a
8	CEBPB	chr7:147571771-147571933	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr7:147576473-147576808	HepG2	liver:	n/a	chr7:147576642-147576653 chr7:147576642-147576655 chr7:147576644-147576653 chr7:147576643-147576654
10	CEBPB	chr7:147576540-147576763	A549	lung:	n/a	chr7:147576642-147576653 chr7:147576642-147576655 chr7:147576644-147576653 chr7:147576643-147576654
11	CEBPB	chr7:147552672-147552872	HepG2	liver:	n/a	chr7:147552735-147552746 chr7:147552796-147552807
12	CEBPB	chr7:147510157-147510402	HepG2	liver:	n/a	n/a
13	CEBPB	chr7:147583840-147584110	HepG2	liver:	n/a	n/a
14	CEBPB	chr7:147576494-147576783	IMR90	lung:	n/a	chr7:147576642-147576653 chr7:147576642-147576655 chr7:147576644-147576653 chr7:147576643-147576654
15	CEBPZ	chr7:147581011-147581064	HepG2	liver:	n/a	n/a
16	CTCF	chr7:147576903-147576920	Lung_OC	lung:	n/a	n/a
17	CTCF	chr7:147503380-147503530	HMEC	breast:	n/a	n/a
18	CTCF	chr7:147486700-147486850	WERI-Rb-1	eye:	n/a	n/a
19	CTCF	chr7:147528544-147528640	LNCaP	prostate:	n/a	n/a
20	CTCF	chr7:147486666-147486856	Medullo	brain:	n/a	n/a
21	CTCF	chr7:147486744-147486857	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr7:147503420-147503570	HEK293	kidney:	n/a	n/a
23	CTCF	chr7:147486704-147486857	ProgFib	skin:	n/a	n/a
24	CTCF	chr7:147486700-147486850	BE2_C	brain:	n/a	n/a
25	CTCF	chr7:147503300-147503450	RPTEC	kidney:	n/a	n/a
26	CTCF	chr7:147503380-147503530	MCF-7	breast:	n/a	n/a
27	CTCF	chr7:147486660-147486810	AG10803	skin:	n/a	n/a
28	CTCF	chr7:147503380-147503530	HRE	kidney:	n/a	n/a
29	CTCF	chr7:147486680-147486830	AG10803	skin:	n/a	n/a
30	CTCF	chr7:147486708-147486869	MCF-7	breast:	n/a	n/a
31	CTCF	chr7:147486723-147486863	LNCaP	prostate:	n/a	n/a
32	CTCF	chr7:147486753-147486840	A549	lung:	n/a	n/a
33	CTCF	chr7:147560349-147560385	Lung_OC	lung:	n/a	n/a
34	CTCF	chr7:147524360-147524510	HVMF	connective:	n/a	n/a
35	CTCF	chr7:147486757-147486834	HepG2	liver:	n/a	n/a
36	CTCF	chr7:147503420-147503570	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr7:147486680-147486830	NB4	blood:	n/a	n/a
38	CTCF	chr7:147486691-147486891	GM12878	blood:	n/a	n/a
39	CTCF	chr7:147528579-147528619	MCF-7	breast:	n/a	n/a
40	CTCF	chr7:147503380-147503530	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr7:147486701-147486885	LNCaP	prostate:	n/a	n/a
42	CTCF	chr7:147486660-147486810	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr7:147486708-147486867	MCF-7	breast:	n/a	n/a
44	CTCF	chr7:147500420-147500570	SK-N-SH_RA	brain:	n/a	chr7:147500508-147500516 chr7:147500509-147500522
45	CTCF	chr7:147503360-147503510	MCF-7	breast:	n/a	n/a
46	CTCF	chr7:147486739-147486840	MCF-7	breast:	n/a	n/a
47	CTCF	chr7:147486727-147486869	Fibrobl	skin:	n/a	n/a
48	CTCF	chr7:147532880-147533030	AG09309	skin:	n/a	n/a
49	CTCF	chr7:147486640-147486790	AG09309	skin:	n/a	n/a
50	CTCF	chr7:147486760-147486910	AG04449	skin:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:147500722-147500772	GM12878	blood:	n/a
2	chr7:147500722-147500772	AG04449	skin:	fetal
3	chr7:147500503-147500553	ProgFib	skin:	n/a
4	chr7:147500722-147500772	MCF10A-Er-Src	breast:	n/a
5	chr7:147500503-147500553	RPTEC	kidney:	n/a
6	chr7:147500722-147500772	PANC-1	pancreas:	n/a
7	chr7:147500722-147500772	HEK293	kidney:	embryo
8	chr7:147500722-147500772	AG09319	gingival:	n/a
9	chr7:147500503-147500553	HEK293	kidney:	embryo
10	chr7:147500503-147500553	SKMC	muscle:	n/a
11	chr7:147500503-147500553	HUVEC	blood vessel:	n/a
12	chr7:147500503-147500553	ovcar-3	ovarian:	n/a
13	chr7:147500503-147500553	NT2-D1	testis:	n/a
14	chr7:147500722-147500772	HRPEpiC	eye:	n/a
15	chr7:147500722-147500772	A549	lung:	n/a
16	chr7:147500722-147500772	AG09309	skin:	n/a
17	chr7:147500503-147500553	GM06990	blood:	n/a
18	chr7:147500503-147500553	T-47D	breast:	n/a
19	chr7:147500503-147500553	AG10803	skin:	n/a
20	chr7:147500503-147500553	BE2_C	brain:	n/a
21	chr7:147500503-147500553	Jurkat	blood:	n/a
22	chr7:147500722-147500772	HRCEpiC	kidney:	n/a
23	chr7:147500503-147500553	HNPCEpiC	eye:	n/a
24	chr7:147500722-147500772	HCT-116	colon:	n/a
25	chr7:147500722-147500772	K562	blood:	n/a
26	chr7:147500503-147500553	PFSK-1	brain:	n/a
27	chr7:147500722-147500772	Caco-2	colon:	n/a
28	chr7:147500503-147500553	H1-hESC	embryonic stem cell:	embryo
29	chr7:147500503-147500553	NH-A	brain:	n/a
30	chr7:147500722-147500772	LNCaP	prostate:	n/a
31	chr7:147500503-147500553	HCT-116	colon:	n/a
32	chr7:147500503-147500553	MCF-7	breast:	n/a
33	chr7:147500503-147500553	HRCEpiC	kidney:	n/a
34	chr7:147500503-147500553	HepG2	liver:	n/a
35	chr7:147500503-147500553	SK-N-SH_RA	brain:	n/a
36	chr7:147500503-147500553	Caco-2	colon:	n/a
37	chr7:147500722-147500772	SAEC	small airway:	n/a
38	chr7:147500503-147500553	HMEC	breast:	n/a
39	chr7:147500722-147500772	NHBE	bronchial:	n/a
40	chr7:147500722-147500772	HIPEpiC	eye:	n/a
41	chr7:147500503-147500553	HCF	heart:	n/a
42	chr7:147500503-147500553	PANC-1	pancreas:	n/a
43	chr7:147500722-147500772	GM12892	blood:	n/a
44	chr7:147500722-147500772	HepG2	liver:	n/a
45	chr7:147500722-147500772	HCPEpiC	choroid plexus:	n/a
46	chr7:147500722-147500772	HEEpiC	esophagus:	n/a
47	chr7:147500503-147500553	HCPEpiC	choroid plexus:	n/a
48	chr7:147500503-147500553	HEEpiC	esophagus:	n/a
49	chr7:147500503-147500553	NHDF-neo	bronchial:	n/a
50	chr7:147500722-147500772	MCF-7	breast:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:57920819..57922347-chr7:147503999..147506112,2	MCF-7	breast:
2	chr7:147545107..147547622-chr7:147549641..147552092,2	K562	blood:
3	chr3:105481713..105484437-chr7:147483253..147485905,2	MCF-7	breast:
4	chr7:147468495..147470634-chr7:147474029..147476158,2	K562	blood:
5	chr11:39750814..39753511-chr7:147523706..147526586,2	MCF-7	breast:

No data

Variant related genes	Relation type
RNA5SP249	TF binding region
RNU6-1184P	TF binding region
RNA5SP249	CpG island
RNU6-1184P	CpG island
ENSG00000251936	chromatin interactions
ENSG00000264020	chromatin interactions

Extended variants
information (count: 2529 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:2529 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs851674	chr7:147471710-147471711	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs535717454	chr7:147471711-147471712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148834433	chr7:147471713-147471714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs371921145	chr7:147471714-147471715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs76600573	chr7:147471725-147471726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573897540	chr7:147471849-147471850	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs78663253	chr7:147471861-147471862	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs553163425	chr7:147471876-147471877	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs151017213	chr7:147471925-147471926	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs545558167	chr7:147471975-147471976	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs75257950	chr7:147471994-147471995	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs547497577	chr7:147472026-147472027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186584203	chr7:147472043-147472044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs140894204	chr7:147472053-147472054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150157839	chr7:147472070-147472071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs75541662	chr7:147472095-147472096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142693468	chr7:147472218-147472219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553630071	chr7:147472219-147472220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs374188652	chr7:147472321-147472322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs111749761	chr7:147472322-147472323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200939936	chr7:147472333-147472334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs202203208	chr7:147472335-147472336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs192248857	chr7:147472352-147472353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs11767652	chr7:147472376-147472377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2373184	chr7:147472397-147472398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs2373185	chr7:147472399-147472400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs2373186	chr7:147472402-147472403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs373798715	chr7:147472413-147472414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368490416	chr7:147472415-147472416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs2373187	chr7:147472430-147472431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372262959	chr7:147472451-147472452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376836947	chr7:147472456-147472457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs10554154	chr7:147472457-147472458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201348284	chr7:147472514-147472515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532577619	chr7:147472519-147472520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs552306572	chr7:147472572-147472573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs571031415	chr7:147472576-147472577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181754034	chr7:147472663-147472664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs199642271	chr7:147472678-147472679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs550587363	chr7:147472709-147472710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs567132190	chr7:147472769-147472770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs536594251	chr7:147472786-147472787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576180474	chr7:147472823-147472824	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs572005471	chr7:147472828-147472829	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs573132255	chr7:147472851-147472852	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs540203747	chr7:147472861-147472862	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs186780187	chr7:147472866-147472867	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs558756897	chr7:147472874-147472875	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs575823838	chr7:147472896-147472897	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs544363495	chr7:147472905-147472906	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pancreatitis	21956041	CNVD
Acute myeloid leukemia	16864856	CNVD
Gastric cancer	16891809	CNVD
Lung cancer	17086460	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20808228	CNVD
Schizophrenia	20838587	CNVD
Schizophrenia	20718829	CNVD
Neuropsychiatric disorder	21827697	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Autism	20964600	CNVD
Epilepsy	17646849	CNVD
Mental retardation	19896112	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD

Chromatin state (count:154 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:147461200-147472800	Weak transcription	Brain Angular Gyrus	brain
2	chr7:147468800-147472600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr7:147468800-147472600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr7:147468800-147473000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr7:147470000-147472600	Weak transcription	Brain Cingulate Gyrus	brain
6	chr7:147470400-147471800	Weak transcription	Brain Hippocampus Middle	brain
7	chr7:147471400-147472800	Weak transcription	Brain Substantia Nigra	brain
8	chr7:147471800-147472000	ZNF genes & repeats	Brain Hippocampus Middle	brain
9	chr7:147472000-147472800	Weak transcription	Brain Hippocampus Middle	brain
10	chr7:147472600-147473200	Enhancers	Brain Cingulate Gyrus	brain
11	chr7:147472600-147473400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr7:147472600-147473600	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr7:147472800-147473200	Flanking Active TSS	Brain Hippocampus Middle	brain
14	chr7:147472800-147473400	Enhancers	Brain Substantia Nigra	brain
15	chr7:147472800-147473600	Enhancers	Brain Angular Gyrus	brain
16	chr7:147473000-147473400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr7:147473200-147473800	Enhancers	Brain Hippocampus Middle	brain
18	chr7:147473200-147474600	Weak transcription	Brain Cingulate Gyrus	brain
19	chr7:147473400-147478000	Weak transcription	Brain Substantia Nigra	brain
20	chr7:147473800-147477800	Weak transcription	Brain Hippocampus Middle	brain
21	chr7:147474600-147475200	Enhancers	Brain Cingulate Gyrus	brain
22	chr7:147477800-147478000	Enhancers	Brain Hippocampus Middle	brain
23	chr7:147478000-147478600	Enhancers	Brain Substantia Nigra	brain
24	chr7:147485000-147485200	Enhancers	Brain Substantia Nigra	brain
25	chr7:147485200-147485800	Weak transcription	Brain Substantia Nigra	brain
26	chr7:147485800-147486800	Enhancers	Brain Substantia Nigra	brain
27	chr7:147486200-147486800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr7:147486400-147486800	Enhancers	Brain Hippocampus Middle	brain
29	chr7:147493400-147493800	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr7:147493600-147494400	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr7:147493800-147494000	Enhancers	Brain Substantia Nigra	brain
32	chr7:147494000-147494400	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr7:147494000-147494400	Weak transcription	Brain Substantia Nigra	brain
34	chr7:147494400-147494600	Enhancers	Brain Substantia Nigra	brain
35	chr7:147494600-147506200	Weak transcription	Brain Substantia Nigra	brain
36	chr7:147495000-147495600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr7:147495000-147496600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr7:147495200-147496000	Enhancers	Fetal Lung	lung
39	chr7:147495800-147496600	Enhancers	Osteobl	bone
40	chr7:147496000-147500200	Weak transcription	Fetal Lung	lung
41	chr7:147500200-147501600	Enhancers	Fetal Lung	lung
42	chr7:147500400-147500800	Enhancers	Fetal Stomach	stomach
43	chr7:147500400-147501000	Enhancers	Ovary	ovary
44	chr7:147500400-147501600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr7:147501000-147501600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr7:147501000-147506200	Weak transcription	Ovary	ovary
47	chr7:147501600-147506400	Weak transcription	Fetal Lung	lung
48	chr7:147506000-147506800	Enhancers	Fetal Stomach	stomach
49	chr7:147506000-147507000	Enhancers	Brain Anterior Caudate	brain
50	chr7:147506200-147506800	Enhancers	Brain Substantia Nigra	brain

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