Variant report

Variant	nsv889395
Chromosome Location	chr7:146848251-146969389
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:413)
CpG islands
(count:122)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:413 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:146873275-146873410	K562	blood:	n/a	n/a
2	ARID3A	chr7:146855481-146855483	K562	blood:	n/a	n/a
3	ARID3A	chr7:146942453-146942657	K562	blood:	n/a	n/a
4	ATF2	chr7:146850658-146851014	GM12878	blood:	n/a	n/a
5	ATF2	chr7:146850699-146851048	GM12878	blood:	n/a	n/a
6	BACH1	chr7:146858480-146858869	H1-hESC	embryonic stem cell:	n/a	chr7:146858693-146858707
7	BHLHE40	chr7:146850941-146850943	GM12878	blood:	n/a	n/a
8	CEBPB	chr7:146890827-146890833	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr7:146947772-146947947	HepG2	liver:	n/a	chr7:146947806-146947817
10	CEBPB	chr7:146942460-146942723	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr7:146942436-146942788	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr7:146942500-146942650	HFF-Myc	foreskin:	n/a	n/a
13	CTCF	chr7:146942460-146942610	NHEK	skin:	n/a	n/a
14	CTCF	chr7:146947180-146947330	A549	lung:	n/a	n/a
15	CTCF	chr7:146947220-146947370	HRPEpiC	eye:	n/a	n/a
16	CTCF	chr7:146942500-146942650	HepG2	liver:	n/a	n/a
17	CTCF	chr7:146942480-146942630	GM12868	blood:	n/a	n/a
18	CTCF	chr7:146942424-146942700	GM12892	blood:	n/a	n/a
19	CTCF	chr7:146942437-146942684	Spleen_OC	spleen:	n/a	n/a
20	CTCF	chr7:146942460-146942610	GM12870	blood:	n/a	n/a
21	CTCF	chr7:146942375-146942771	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr7:146942500-146942650	AoAF	blood vessel:	n/a	n/a
23	CTCF	chr7:146947103-146947349	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr7:146947200-146947350	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr7:146942440-146942590	A549	lung:	n/a	n/a
26	CTCF	chr7:146942480-146942630	SAEC	small airway:	n/a	n/a
27	CTCF	chr7:146947200-146947350	HMF	breast:	n/a	n/a
28	CTCF	chr7:146947120-146947270	HCPEpiC	choroid plexus:	n/a	n/a
29	CTCF	chr7:146942540-146942690	K562	blood:	n/a	n/a
30	CTCF	chr7:146942401-146942708	T-47D	breast:	n/a	n/a
31	CTCF	chr7:146942460-146942610	WI-38	lung:	n/a	n/a
32	CTCF	chr7:146942351-146942755	GM12878	blood:	n/a	n/a
33	CTCF	chr7:146942500-146942650	AG04450	lung:	n/a	n/a
34	CTCF	chr7:146942520-146942670	AoAF	blood vessel:	n/a	n/a
35	CTCF	chr7:146942500-146942650	NHLF	lung:	n/a	n/a
36	CTCF	chr7:146947240-146947390	HCM	heart:	n/a	n/a
37	CTCF	chr7:146942455-146942684	GM10266	blood:	n/a	n/a
38	CTCF	chr7:146942429-146942680	GM10248	blood:	n/a	n/a
39	CTCF	chr7:146942500-146942650	AG04449	skin:	n/a	n/a
40	CTCF	chr7:146942463-146942675	HepG2	liver:	n/a	n/a
41	CTCF	chr7:146942480-146942630	HL-60	blood:	n/a	n/a
42	CTCF	chr7:146947180-146947330	HPF	lung:	n/a	n/a
43	CTCF	chr7:146947160-146947310	AG10803	skin:	n/a	n/a
44	CTCF	chr7:146942520-146942670	AG04450	lung:	n/a	n/a
45	CTCF	chr7:146942480-146942630	HMF	breast:	n/a	n/a
46	CTCF	chr7:146942161-146942933	SK-N-SH	brain:	n/a	n/a
47	CTCF	chr7:146942380-146942530	WI-38	lung:	n/a	n/a
48	CTCF	chr7:146942420-146942570	HVMF	connective:	n/a	n/a
49	CTCF	chr7:146942440-146942590	GM12865	blood:	n/a	n/a
50	CTCF	chr7:146942480-146942630	GM12874	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:146897691-146897741	HPAEpiC	pulmonary alveolar:	n/a
2	chr7:146904205-146904255	H1-hESC	embryonic stem cell:	embryo
3	chr7:146897691-146897741	BJ	skin:	n/a
4	chr7:146904205-146904255	HRCEpiC	kidney:	n/a
5	chr7:146897691-146897741	CMK	blood:	n/a
6	chr7:146904205-146904255	SKMC	muscle:	n/a
7	chr7:146904205-146904255	SK-N-MC	brain:	n/a
8	chr7:146904205-146904255	ProgFib	skin:	n/a
9	chr7:146904205-146904255	SAEC	small airway:	n/a
10	chr7:146904205-146904255	PANC-1	pancreas:	n/a
11	chr7:146897691-146897741	T-47D	breast:	n/a
12	chr7:146897691-146897741	U87	brain:	n/a
13	chr7:146904205-146904255	AoSMC	blood vessel:	n/a
14	chr7:146904205-146904255	HNPCEpiC	eye:	n/a
15	chr7:146904205-146904255	HCM	heart:	n/a
16	chr7:146904205-146904255	BJ	skin:	n/a
17	chr7:146904205-146904255	GM12891	blood:	n/a
18	chr7:146904205-146904255	MCF-7	breast:	n/a
19	chr7:146904205-146904255	Hela-S3	cervix:	n/a
20	chr7:146897691-146897741	AG10803	skin:	n/a
21	chr7:146904205-146904255	MCF10A-Er-Src	breast:	n/a
22	chr7:146897691-146897741	ECC-1	luminal epithelium:	n/a
23	chr7:146897691-146897741	HUVEC	blood vessel:	n/a
24	chr7:146897691-146897741	K562	blood:	n/a
25	chr7:146904205-146904255	SK-N-SH	brain:	n/a
26	chr7:146897691-146897741	LNCaP	prostate:	n/a
27	chr7:146904205-146904255	GM06990	blood:	n/a
28	chr7:146897691-146897741	BE2_C	brain:	n/a
29	chr7:146897691-146897741	H1-hESC	embryonic stem cell:	embryo
30	chr7:146904205-146904255	HepG2	liver:	n/a
31	chr7:146897691-146897741	HEEpiC	esophagus:	n/a
32	chr7:146904205-146904255	HPAEpiC	pulmonary alveolar:	n/a
33	chr7:146897691-146897741	Hela-S3	cervix:	n/a
34	chr7:146904205-146904255	NHBE	bronchial:	n/a
35	chr7:146897691-146897741	HCPEpiC	choroid plexus:	n/a
36	chr7:146904205-146904255	HUVEC	blood vessel:	n/a
37	chr7:146904205-146904255	BE2_C	brain:	n/a
38	chr7:146897691-146897741	SKMC	muscle:	n/a
39	chr7:146897691-146897741	HIPEpiC	eye:	n/a
40	chr7:146904205-146904255	HRE	kidney:	n/a
41	chr7:146904205-146904255	IMR90	lung:	fetal
42	chr7:146897691-146897741	AG09319	gingival:	n/a
43	chr7:146897691-146897741	ProgFib	skin:	n/a
44	chr7:146904205-146904255	HCF	heart:	n/a
45	chr7:146904205-146904255	SK-N-SH_RA	brain:	n/a
46	chr7:146904205-146904255	GM12878	blood:	n/a
47	chr7:146897691-146897741	NB4	blood:	n/a
48	chr7:146897691-146897741	RPTEC	kidney:	n/a
49	chr7:146904205-146904255	K562	blood:	n/a
50	chr7:146897691-146897741	PrEC	prostate:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:146864798..146866603-chr7:146876111..146877910,2	K562	blood:
2	chr7:146945142..146947426-chr7:146947550..146950265,2	K562	blood:
3	chr7:146864798..146866603-chr7:146876111..146877910,2	K562	blood:
4	chr7:146945142..146947426-chr7:146947550..146950265,2	K562	blood:
5	chr7:146920592..146922587-chr7:146928456..146931427,2	K562	blood:
6	chr7:146920592..146922587-chr7:146928456..146931427,2	K562	blood:
7	chr7:146947046..146947712-chr7:147780872..147781389,2	MCF-7	breast:
8	chr7:146963308..146964971-chr7:147095158..147097762,2	MCF-7	breast:
9	chr7:146913926..146916451-chr7:146918952..146920556,2	K562	blood:
10	chr7:146433613..146434480-chr7:146942002..146942841,3	MCF-7	breast:
11	chr7:146913926..146916451-chr7:146918952..146920556,2	K562	blood:
12	chr7:146942052..146943007-chr7:147780653..147781865,8	MCF-7	breast:

(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: 1115 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:1115 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10500170	chr7:146848251-146848252	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs12670106	chr7:146848333-146848334	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs372099322	chr7:146848396-146848397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs147928066	chr7:146848408-146848409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs181488153	chr7:146848420-146848421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs140412432	chr7:146848438-146848439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564398814	chr7:146848444-146848445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs568467231	chr7:146848449-146848450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537444304	chr7:146848464-146848465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554178162	chr7:146848469-146848470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs373376355	chr7:146848488-146848489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186216426	chr7:146848489-146848490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs114046207	chr7:146848490-146848491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576979264	chr7:146848503-146848504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs545931629	chr7:146848508-146848509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs562969872	chr7:146848636-146848637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142089981	chr7:146848691-146848692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs151149079	chr7:146848705-146848706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562091225	chr7:146848733-146848734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs527947979	chr7:146848751-146848752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs112802437	chr7:146848772-146848773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs202118538	chr7:146848779-146848780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs75636496	chr7:146848788-146848789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548083893	chr7:146848795-146848796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs76879206	chr7:146848844-146848845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs189495115	chr7:146848855-146848856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs550153431	chr7:146848886-146848887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs140058517	chr7:146848904-146848905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs547777794	chr7:146848929-146848930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs375249532	chr7:146848932-146848933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs372625790	chr7:146848940-146848941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs566187364	chr7:146849002-146849003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs368334165	chr7:146849028-146849029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs547756745	chr7:146849037-146849038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs180686002	chr7:146849074-146849075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs185071613	chr7:146849131-146849132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs375623016	chr7:146849210-146849211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs115397192	chr7:146849216-146849217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565026157	chr7:146849232-146849233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs570706642	chr7:146849259-146849260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539613033	chr7:146849287-146849288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191018222	chr7:146849288-146849289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556424447	chr7:146849306-146849307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs576580366	chr7:146849333-146849334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs150291314	chr7:146849336-146849337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs532004335	chr7:146849338-146849339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555762824	chr7:146849417-146849418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs75831681	chr7:146849440-146849441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs541315370	chr7:146849457-146849458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs564798082	chr7:146849494-146849495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:146846400-146850600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:146848800-146849200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr7:146850000-146851000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr7:146850600-146851000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr7:146861200-146862200	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr7:146867800-146868400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr7:146870800-146871000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr7:146879600-146880800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr7:146880400-146880800	Enhancers	Brain Germinal Matrix	brain
10	chr7:146880400-146880800	Enhancers	Fetal Lung	lung
11	chr7:146880400-146881200	Enhancers	Fetal Brain Male	brain
12	chr7:146885200-146885600	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr7:146885200-146886000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr7:146887200-146887600	Enhancers	Fetal Brain Male	brain
15	chr7:146889400-146889600	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr7:146889400-146889800	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr7:146889600-146890600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr7:146889800-146890200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr7:146889800-146890600	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr7:146890200-146891000	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr7:146890400-146890600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr7:146890400-146891000	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr7:146890600-146891000	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr7:146890600-146897200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr7:146894000-146894800	Active TSS	Hela-S3	cervix
26	chr7:146894200-146895000	Active TSS	A549	lung
27	chr7:146894400-146894800	Active TSS	Ovary	ovary
28	chr7:146894400-146894800	Active TSS	HepG2	liver
29	chr7:146894800-146897000	Weak transcription	Ovary	ovary
30	chr7:146897000-146897600	Enhancers	Fetal Brain Female	brain
31	chr7:146897000-146897600	Enhancers	Fetal Lung	lung
32	chr7:146897000-146897600	Enhancers	Ovary	ovary
33	chr7:146897200-146897600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr7:146897200-146897600	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr7:146897600-146898600	Weak transcription	Fetal Lung	lung
36	chr7:146897600-146898600	Weak transcription	Ovary	ovary
37	chr7:146898600-146898800	Enhancers	Fetal Lung	lung
38	chr7:146898600-146898800	Enhancers	Ovary	ovary
39	chr7:146904200-146905000	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr7:146904200-146905200	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr7:146905000-146905200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
42	chr7:146905000-146905400	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr7:146905000-146905600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr7:146905000-146905600	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr7:146905000-146905600	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr7:146905200-146905400	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr7:146905400-146905600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
48	chr7:146909400-146909800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr7:146932800-146933400	Enhancers	Brain Cingulate Gyrus	brain
50	chr7:146932800-146933400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain

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