Variant report

Variant	nsv889396
Chromosome Location	chr7:146854133-147035067
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:530)
CpG islands
(count:124)
Chromatin interactive
region (count:18)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:530 , 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	ARID3A	chr7:146942453-146942657	K562	blood:	n/a	n/a
2	ARID3A	chr7:146855481-146855483	K562	blood:	n/a	n/a
3	ARID3A	chr7:146873275-146873410	K562	blood:	n/a	n/a
4	BACH1	chr7:146858480-146858869	H1-hESC	embryonic stem cell:	n/a	chr7:146858693-146858707
5	CEBPB	chr7:146947772-146947947	HepG2	liver:	n/a	chr7:146947806-146947817
6	CEBPB	chr7:146976578-146977316	HepG2	liver:	n/a	n/a
7	CEBPB	chr7:146983597-146983710	HepG2	liver:	n/a	chr7:146983658-146983669 chr7:146983636-146983653 chr7:146983657-146983668
8	CEBPB	chr7:146890827-146890833	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr7:146942460-146942723	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr7:146942436-146942788	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr7:146942460-146942610	NHEK	skin:	n/a	n/a
12	CTCF	chr7:146942440-146942590	GM12865	blood:	n/a	n/a
13	CTCF	chr7:146947180-146947330	NB4	blood:	n/a	n/a
14	CTCF	chr7:146947200-146947350	HA-sp	spinal cord:	n/a	n/a
15	CTCF	chr7:146942500-146942650	HVMF	connective:	n/a	n/a
16	CTCF	chr7:146942460-146942610	MCF-7	breast:	n/a	n/a
17	CTCF	chr7:146942520-146942670	BJ	skin:	n/a	n/a
18	CTCF	chr7:146947180-146947330	HAc	cerebellar:	n/a	n/a
19	CTCF	chr7:146942421-146942723	MCF-7	breast:	n/a	n/a
20	CTCF	chr7:146942455-146942684	GM10266	blood:	n/a	n/a
21	CTCF	chr7:146942300-146942450	NHLF	lung:	n/a	n/a
22	CTCF	chr7:146942439-146942700	Medullo	brain:	n/a	n/a
23	CTCF	chr7:146942500-146942650	MCF-7	breast:	n/a	n/a
24	CTCF	chr7:146942500-146942650	GM12873	blood:	n/a	n/a
25	CTCF	chr7:146942500-146942650	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr7:146942468-146942667	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr7:146942500-146942650	GM12875	blood:	n/a	n/a
28	CTCF	chr7:146947180-146947330	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr7:146942500-146942650	NB4	blood:	n/a	n/a
30	CTCF	chr7:146942161-146942933	SK-N-SH	brain:	n/a	n/a
31	CTCF	chr7:146942520-146942670	GM12872	blood:	n/a	n/a
32	CTCF	chr7:146942425-146942701	MCF-7	breast:	n/a	n/a
33	CTCF	chr7:146942500-146942650	HEEpiC	esophagus:	n/a	n/a
34	CTCF	chr7:146942475-146942673	HepG2	liver:	n/a	n/a
35	CTCF	chr7:146942460-146942610	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr7:146947220-146947370	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr7:146942540-146942690	SAEC	small airway:	n/a	n/a
38	CTCF	chr7:146942480-146942630	HepG2	liver:	n/a	n/a
39	CTCF	chr7:146947180-146947330	HPF	lung:	n/a	n/a
40	CTCF	chr7:146942480-146942630	HCFaa	heart:	n/a	n/a
41	CTCF	chr7:146947180-146947330	A549	lung:	n/a	n/a
42	CTCF	chr7:146942500-146942650	GM12865	blood:	n/a	n/a
43	CTCF	chr7:146942480-146942630	HMEC	breast:	n/a	n/a
44	CTCF	chr7:146942520-146942670	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr7:146942373-146942754	HepG2	liver:	n/a	n/a
46	CTCF	chr7:146942460-146942610	WI-38	lung:	n/a	n/a
47	CTCF	chr7:146942540-146942690	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr7:146942440-146942590	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr7:146942492-146942665	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr7:146942480-146942630	AG10803	skin:	n/a	n/a

(count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:146904205-146904255	HMEC	breast:	n/a
2	chr7:146897691-146897741	HCF	heart:	n/a
3	chr7:146904205-146904255	HMEC	breast:	n/a
4	chr7:146897691-146897741	HCF	heart:	n/a
5	chr7:146897691-146897741	ovcar-3	ovarian:	n/a
6	chr7:146897691-146897741	GM12878	blood:	n/a
7	chr7:146904205-146904255	SK-N-SH_RA	brain:	n/a
8	chr7:146897691-146897741	AG09309	skin:	n/a
9	chr7:146897691-146897741	GM12892	blood:	n/a
10	chr7:146904205-146904255	U87	brain:	n/a
11	chr7:146897691-146897741	PANC-1	pancreas:	n/a
12	chr7:146904205-146904255	RPTEC	kidney:	n/a
13	chr7:146904205-146904255	GM12892	blood:	n/a
14	chr7:146897691-146897741	HEEpiC	esophagus:	n/a
15	chr7:146897691-146897741	GM06990	blood:	n/a
16	chr7:146904205-146904255	A549	lung:	n/a
17	chr7:146897691-146897741	GM19239	blood:	n/a
18	chr7:146897691-146897741	HNPCEpiC	eye:	n/a
19	chr7:146897691-146897741	K562	blood:	n/a
20	chr7:146904205-146904255	Hela-S3	cervix:	n/a
21	chr7:146904205-146904255	PANC-1	pancreas:	n/a
22	chr7:146897691-146897741	HEK293	kidney:	embryo
23	chr7:146904205-146904255	GM19239	blood:	n/a
24	chr7:146904205-146904255	SAEC	small airway:	n/a
25	chr7:146897691-146897741	HAEpiC	amniotic membrane:	n/a
26	chr7:146904205-146904255	NT2-D1	testis:	n/a
27	chr7:146904205-146904255	Caco-2	colon:	n/a
28	chr7:146904205-146904255	MCF-7	breast:	n/a
29	chr7:146897691-146897741	Hela-S3	cervix:	n/a
30	chr7:146897691-146897741	AG04449	skin:	fetal
31	chr7:146904205-146904255	HRCEpiC	kidney:	n/a
32	chr7:146897691-146897741	BE2_C	brain:	n/a
33	chr7:146897691-146897741	NHDF-neo	bronchial:	n/a
34	chr7:146904205-146904255	HEEpiC	esophagus:	n/a
35	chr7:146897691-146897741	HCT-116	colon:	n/a
36	chr7:146897691-146897741	Caco-2	colon:	n/a
37	chr7:146904205-146904255	H1-hESC	embryonic stem cell:	embryo
38	chr7:146897691-146897741	HepG2	liver:	n/a
39	chr7:146897691-146897741	HL-60	blood:	n/a
40	chr7:146897691-146897741	HCPEpiC	choroid plexus:	n/a
41	chr7:146904205-146904255	AG09319	gingival:	n/a
42	chr7:146904205-146904255	GM12891	blood:	n/a
43	chr7:146897691-146897741	HRPEpiC	eye:	n/a
44	chr7:146904205-146904255	GM06990	blood:	n/a
45	chr7:146904205-146904255	AG04450	lung:	fetal
46	chr7:146904205-146904255	ECC-1	luminal epithelium:	n/a
47	chr7:146897691-146897741	HUVEC	blood vessel:	n/a
48	chr7:146897691-146897741	HRCEpiC	kidney:	n/a
49	chr7:146904205-146904255	AG04449	skin:	fetal
50	chr7:146904205-146904255	T-47D	breast:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:146993664..146995748-chr7:147006294..147008294,2	MCF-7	breast:
2	chr7:146864798..146866603-chr7:146876111..146877910,2	K562	blood:
3	chr7:146945142..146947426-chr7:146947550..146950265,2	K562	blood:
4	chr7:146942052..146943007-chr7:147780653..147781865,8	MCF-7	breast:
5	chr7:146989620..146992429-chr7:146994596..146997108,3	K562	blood:
6	chr7:146920592..146922587-chr7:146928456..146931427,2	K562	blood:
7	chr7:146913926..146916451-chr7:146918952..146920556,2	K562	blood:
8	chr7:146920592..146922587-chr7:146928456..146931427,2	K562	blood:
9	chr7:146945142..146947426-chr7:146947550..146950265,2	K562	blood:
10	chr7:146993664..146995748-chr7:147006294..147008294,2	MCF-7	breast:
11	chr7:147018041..147019987-chr7:147042337..147044392,2	K562	blood:
12	chr1:83035755..83036717-chr7:147026373..147027195,2	MCF-7	breast:
13	chr7:146433613..146434480-chr7:146942002..146942841,3	MCF-7	breast:
14	chr7:146989620..146992429-chr7:146994596..146997108,3	K562	blood:
15	chr7:146963308..146964971-chr7:147095158..147097762,2	MCF-7	breast:
16	chr7:146913926..146916451-chr7:146918952..146920556,2	K562	blood:
17	chr7:146947046..146947712-chr7:147780872..147781389,2	MCF-7	breast:
18	chr7:146864798..146866603-chr7:146876111..146877910,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C7orf33-7	chr7:146864436-146864664	NONHSAT123954

No data

Variant related genes	Relation type
RANP2	TF binding region
RANP2	CpG island

Extended variants
information (count: 1974 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:1974 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117439216	chr7:146860062-146860063	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs112361031	chr7:146860084-146860085	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs547155002	chr7:146860086-146860087	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs546156283	chr7:146860088-146860089	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs558427642	chr7:146860212-146860213	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs569097758	chr7:146860221-146860222	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs187306897	chr7:146861206-146861207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs147911101	chr7:146861220-146861221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs569140870	chr7:146861249-146861250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs570536418	chr7:146861318-146861319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs369944701	chr7:146861364-146861365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs192757603	chr7:146861390-146861391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs572304817	chr7:146861434-146861435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs141637586	chr7:146861446-146861447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs559800552	chr7:146861450-146861451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs183165097	chr7:146861462-146861463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs187656551	chr7:146861488-146861489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562361063	chr7:146861512-146861513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs531586624	chr7:146861529-146861530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs192569593	chr7:146861598-146861599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs568384207	chr7:146861600-146861601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs185579110	chr7:146861615-146861616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs372061190	chr7:146861647-146861648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs189638586	chr7:146861694-146861695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs147038705	chr7:146861705-146861706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs192492403	chr7:146861706-146861707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs535249495	chr7:146861707-146861708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs35586468	chr7:146861726-146861727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565999848	chr7:146861793-146861794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs184672424	chr7:146861857-146861858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188993012	chr7:146862033-146862034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs576364382	chr7:146862077-146862078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs79371738	chr7:146862130-146862131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs555778305	chr7:146862143-146862144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572440810	chr7:146862148-146862149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs181328158	chr7:146862150-146862151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs141109261	chr7:146862196-146862197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs185032775	chr7:146862758-146862759	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs576115150	chr7:146862803-146862804	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs534723321	chr7:146864474-146864475	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs10261412	chr7:146864487-146864488	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs577570174	chr7:146864525-146864526	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs536695301	chr7:146864526-146864527	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs557204956	chr7:146864528-146864529	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs573880449	chr7:146864555-146864556	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs542385441	chr7:146864596-146864597	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs552764980	chr7:146864635-146864636	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs13309902	chr7:146864656-146864657	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs547903121	chr7:146867803-146867804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs570958567	chr7:146867805-146867806	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Glioblastoma multiforme	18628472	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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:152 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:146861200-146862200	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr7:146867800-146868400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr7:146870800-146871000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr7:146879600-146880800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr7:146880400-146880800	Enhancers	Brain Germinal Matrix	brain
6	chr7:146880400-146880800	Enhancers	Fetal Lung	lung
7	chr7:146880400-146881200	Enhancers	Fetal Brain Male	brain
8	chr7:146885200-146885600	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr7:146885200-146886000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr7:146887200-146887600	Enhancers	Fetal Brain Male	brain
11	chr7:146889400-146889600	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr7:146889400-146889800	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr7:146889600-146890600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr7:146889800-146890200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr7:146889800-146890600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr7:146890200-146891000	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr7:146890400-146890600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr7:146890400-146891000	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr7:146890600-146891000	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr7:146890600-146897200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr7:146894000-146894800	Active TSS	Hela-S3	cervix
22	chr7:146894200-146895000	Active TSS	A549	lung
23	chr7:146894400-146894800	Active TSS	Ovary	ovary
24	chr7:146894400-146894800	Active TSS	HepG2	liver
25	chr7:146894800-146897000	Weak transcription	Ovary	ovary
26	chr7:146897000-146897600	Enhancers	Fetal Brain Female	brain
27	chr7:146897000-146897600	Enhancers	Fetal Lung	lung
28	chr7:146897000-146897600	Enhancers	Ovary	ovary
29	chr7:146897200-146897600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr7:146897200-146897600	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr7:146897600-146898600	Weak transcription	Fetal Lung	lung
32	chr7:146897600-146898600	Weak transcription	Ovary	ovary
33	chr7:146898600-146898800	Enhancers	Fetal Lung	lung
34	chr7:146898600-146898800	Enhancers	Ovary	ovary
35	chr7:146904200-146905000	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr7:146904200-146905200	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr7:146905000-146905200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
38	chr7:146905000-146905400	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr7:146905000-146905600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
40	chr7:146905000-146905600	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr7:146905000-146905600	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr7:146905200-146905400	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr7:146905400-146905600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
44	chr7:146909400-146909800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr7:146932800-146933400	Enhancers	Brain Cingulate Gyrus	brain
46	chr7:146932800-146933400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
47	chr7:146933000-146933400	Enhancers	Brain Anterior Caudate	brain
48	chr7:146933000-146933400	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr7:146942000-146942600	Enhancers	Primary B cells from cord blood	blood
50	chr7:146945200-146945800	Enhancers	ES-I3 Cell Line	embryonic stem cell

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