Variant report

Variant	nsv608011
Chromosome Location	chr7:102127893-102334106
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:6555)
CpG islands
(count:1527)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:6555 , 50 per page) page: 1 2 3 4 5 6 7 ... 132

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102212897-102213097	HepG2	liver:	n/a	n/a
2	ATF2	chr7:102153014-102153393	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr7:102312022-102312401	A549	lung:	n/a	chr7:102312144-102312152
4	ATF3	chr7:102312099-102312242	K562	blood:	n/a	chr7:102312144-102312152
5	ATF3	chr7:102213014-102213188	K562	blood:	n/a	n/a
6	ATF3	chr7:102213014-102213141	GM12878	blood:	n/a	n/a
7	BACH1	chr7:102213021-102213172	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr7:102310144-102310402	GM12878	blood:	n/a	n/a
9	BATF	chr7:102247244-102247556	GM12878	blood:	n/a	n/a
10	BATF	chr7:102211460-102211924	GM12878	blood:	n/a	n/a
11	BATF	chr7:102158383-102158641	GM12878	blood:	n/a	n/a
12	BATF	chr7:102256202-102256653	GM12878	blood:	n/a	n/a
13	BATF	chr7:102211064-102211322	GM12878	blood:	n/a	n/a
14	BATF	chr7:102284603-102285287	GM12878	blood:	n/a	n/a
15	BATF	chr7:102185674-102186087	GM12878	blood:	n/a	n/a
16	BATF	chr7:102285771-102286300	GM12878	blood:	n/a	chr7:102286082-102286093
17	BATF	chr7:102153892-102154083	GM12878	blood:	n/a	n/a
18	BATF	chr7:102185510-102186196	GM12878	blood:	n/a	n/a
19	BATF	chr7:102155784-102156059	GM12878	blood:	n/a	n/a
20	BATF	chr7:102152206-102152651	GM12878	blood:	n/a	n/a
21	BATF	chr7:102214085-102214343	GM12878	blood:	n/a	n/a
22	BATF	chr7:102155274-102155743	GM12878	blood:	n/a	n/a
23	BATF	chr7:102306478-102306740	GM12878	blood:	n/a	n/a
24	BATF	chr7:102155139-102156246	GM12878	blood:	n/a	n/a
25	BATF	chr7:102254253-102254722	GM12878	blood:	n/a	n/a
26	BATF	chr7:102330287-102330744	GM12878	blood:	n/a	n/a
27	BATF	chr7:102179772-102180041	GM12878	blood:	n/a	n/a
28	BATF	chr7:102285752-102286469	GM12878	blood:	n/a	chr7:102286082-102286093
29	BATF	chr7:102254763-102255038	GM12878	blood:	n/a	n/a
30	BATF	chr7:102167226-102167423	GM12878	blood:	n/a	n/a
31	BATF	chr7:102286810-102287040	GM12878	blood:	n/a	n/a
32	BATF	chr7:102251367-102251812	GM12878	blood:	n/a	n/a
33	BATF	chr7:102266316-102266513	GM12878	blood:	n/a	n/a
34	BATF	chr7:102313151-102313476	GM12878	blood:	n/a	n/a
35	BATF	chr7:102278880-102279149	GM12878	blood:	n/a	n/a
36	BATF	chr7:102205933-102206440	GM12878	blood:	n/a	n/a
37	BATF	chr7:102305017-102305524	GM12878	blood:	n/a	n/a
38	BATF	chr7:102157223-102157674	GM12878	blood:	n/a	n/a
39	BATF	chr7:102186661-102187378	GM12878	blood:	n/a	chr7:102186991-102187002
40	BATF	chr7:102234392-102234834	GM12878	blood:	n/a	n/a
41	BATF	chr7:102186680-102187209	GM12878	blood:	n/a	chr7:102186991-102187002
42	BATF	chr7:102233914-102234227	GM12878	blood:	n/a	n/a
43	BATF	chr7:102212695-102213163	GM12878	blood:	n/a	n/a
44	BATF	chr7:102311459-102312701	GM12878	blood:	n/a	n/a
45	BATF	chr7:102187719-102187949	GM12878	blood:	n/a	n/a
46	BATF	chr7:102293584-102293766	GM12878	blood:	n/a	n/a
47	BATF	chr7:102312293-102312492	GM12878	blood:	n/a	n/a
48	BATF	chr7:102135223-102135665	GM12878	blood:	n/a	n/a
49	BATF	chr7:102278828-102279089	GM12878	blood:	n/a	n/a
50	BATF	chr7:102291963-102292217	GM12878	blood:	n/a	n/a

(count:1527 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102155527-102155577	HRE	kidney:	n/a
2	chr7:102327236-102327286	Hela-S3	cervix:	n/a
3	chr7:102155527-102155577	HRE	kidney:	n/a
4	chr7:102327236-102327286	Hela-S3	cervix:	n/a
5	chr7:102313412-102313462	AG10803	skin:	n/a
6	chr7:102161506-102161556	BJ	skin:	n/a
7	chr7:102259241-102259291	HCT-116	colon:	n/a
8	chr7:102332458-102332508	GM06990	blood:	n/a
9	chr7:102212892-102212942	Hela-S3	cervix:	n/a
10	chr7:102327236-102327286	ECC-1	luminal epithelium:	n/a
11	chr7:102312308-102312358	HUVEC	blood vessel:	n/a
12	chr7:102312308-102312358	HCPEpiC	choroid plexus:	n/a
13	chr7:102151231-102151281	Jurkat	blood:	n/a
14	chr7:102132012-102132062	U87	brain:	n/a
15	chr7:102308061-102308111	HEEpiC	esophagus:	n/a
16	chr7:102155527-102155577	GM12891	blood:	n/a
17	chr7:102132012-102132062	HNPCEpiC	eye:	n/a
18	chr7:102134668-102134718	HRPEpiC	eye:	n/a
19	chr7:102312318-102312368	ProgFib	skin:	n/a
20	chr7:102327236-102327286	HRPEpiC	eye:	n/a
21	chr7:102311965-102312015	LNCaP	prostate:	n/a
22	chr7:102212892-102212942	SK-N-MC	brain:	n/a
23	chr7:102308061-102308111	BJ	skin:	n/a
24	chr7:102246378-102246428	AG04450	lung:	fetal
25	chr7:102155527-102155577	BE2_C	brain:	n/a
26	chr7:102151231-102151281	SK-N-MC	brain:	n/a
27	chr7:102327236-102327286	HAEpiC	amniotic membrane:	n/a
28	chr7:102312315-102312365	HCF	heart:	n/a
29	chr7:102312315-102312365	CMK	blood:	n/a
30	chr7:102161506-102161556	NT2-D1	testis:	n/a
31	chr7:102155527-102155577	ProgFib	skin:	n/a
32	chr7:102134668-102134718	GM06990	blood:	n/a
33	chr7:102312331-102312381	PFSK-1	brain:	n/a
34	chr7:102312315-102312365	Caco-2	colon:	n/a
35	chr7:102312315-102312365	BE2_C	brain:	n/a
36	chr7:102312331-102312381	Caco-2	colon:	n/a
37	chr7:102313412-102313462	SK-N-MC	brain:	n/a
38	chr7:102151231-102151281	HUVEC	blood vessel:	n/a
39	chr7:102196182-102196232	PANC-1	pancreas:	n/a
40	chr7:102212892-102212942	HRPEpiC	eye:	n/a
41	chr7:102327236-102327286	SK-N-SH	brain:	n/a
42	chr7:102155527-102155577	HRPEpiC	eye:	n/a
43	chr7:102327236-102327286	ovcar-3	ovarian:	n/a
44	chr7:102313412-102313462	HMEC	breast:	n/a
45	chr7:102134668-102134718	ECC-1	luminal epithelium:	n/a
46	chr7:102312318-102312368	NHDF-neo	bronchial:	n/a
47	chr7:102312331-102312381	HCM	heart:	n/a
48	chr7:102332458-102332508	HUVEC	blood vessel:	n/a
49	chr7:102136524-102136574	SAEC	small airway:	n/a
50	chr7:102134668-102134718	SK-N-SH	brain:	n/a

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RASA4	hsa-miR-335-5p	chr7:102227581-102227605
2	RASA4	hsa-miR-335-5p	chr7:102128407-102128431

Variant related genes	Relation type
ENSG00000270249	TF binding region
ENSG00000228049	TF binding region
ENSG00000238997	TF binding region
RASA4B	TF binding region
ENSG00000272949	TF binding region
UPK3BL	TF binding region
POLR2J2	TF binding region
SPDYE2	TF binding region
ENSG00000205236	TF binding region
RASA4	TF binding region
RASA4DP	TF binding region
POLR2J3	TF binding region
SPDYE2B	TF binding region
ENSG00000238392	TF binding region
ENSG00000270249	CpG island
ENSG00000228049	CpG island
ENSG00000238997	CpG island
RASA4B	CpG island
ENSG00000272949	CpG island
UPK3BL	CpG island
POLR2J2	CpG island
SPDYE2	CpG island
ENSG00000205236	CpG island
RASA4	CpG island
RASA4DP	CpG island
POLR2J3	CpG island
SPDYE2B	CpG island
ENSG00000238392	CpG island

Extended variants
information (count: 2099 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:2099 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369175625	chr7:102128330-102128331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs374604089	chr7:102128371-102128372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570964131	chr7:102128660-102128661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138016001	chr7:102129924-102129925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs112776060	chr7:102129937-102129938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs200860960	chr7:102129944-102129945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs376485509	chr7:102129945-102129946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs535272816	chr7:102129987-102129988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs546859554	chr7:102130002-102130003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs28431891	chr7:102130003-102130004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568183958	chr7:102130059-102130060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535146568	chr7:102130077-102130078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556562581	chr7:102130085-102130086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs74558171	chr7:102130087-102130088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs79154572	chr7:102130089-102130090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs77289711	chr7:102130097-102130098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573051121	chr7:102130108-102130109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540448925	chr7:102130204-102130205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112435681	chr7:102130228-102130229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs57548697	chr7:102130238-102130239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150302855	chr7:102130239-102130240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144880633	chr7:102130240-102130241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs58482585	chr7:102130250-102130251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs542313390	chr7:102130378-102130379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372555271	chr7:102130406-102130407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs28510701	chr7:102130419-102130420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369937855	chr7:102130517-102130518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs62483856	chr7:102131071-102131072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs28688258	chr7:102131182-102131183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs563674336	chr7:102131203-102131204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs62483857	chr7:102131234-102131235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs536223836	chr7:102131235-102131236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530883912	chr7:102131238-102131239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs62483858	chr7:102131243-102131244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs62483859	chr7:102131249-102131250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs62484760	chr7:102131254-102131255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs62484761	chr7:102131429-102131430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552277433	chr7:102131476-102131477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs564832666	chr7:102131533-102131534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528768039	chr7:102131539-102131540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs376745484	chr7:102131850-102131851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs371345497	chr7:102131940-102131941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547189059	chr7:102132033-102132034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201846024	chr7:102132037-102132038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs61561856	chr7:102132155-102132156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs76869716	chr7:102132168-102132169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs77382905	chr7:102132185-102132186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs527777084	chr7:102132215-102132216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs146703683	chr7:102132232-102132233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs59999871	chr7:102132233-102132234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	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
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21509527	CNVD
Schizophrenia	20967226	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Bipolar disorder	19114987	CNVD
abnormal development	18461090	CNVD

Chromatin state (count:1010 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102119400-102134600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr7:102119400-102153000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr7:102119400-102153200	Weak transcription	Ovary	ovary
4	chr7:102134000-102134400	Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr7:102134000-102134400	Active TSS	Hela-S3	cervix
6	chr7:102134400-102134600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
7	chr7:102134400-102134600	Active TSS	Primary T cells fromperipheralblood	blood
8	chr7:102134400-102134600	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
9	chr7:102134400-102134600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr7:102134400-102134600	Active TSS	Fetal Thymus	thymus
11	chr7:102134400-102134800	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr7:102134400-102134800	Active TSS	Primary B cells from peripheral blood	blood
13	chr7:102134400-102134800	Active TSS	Primary T helper cells fromperipheralblood	blood
14	chr7:102134400-102134800	Active TSS	Fetal Brain Female	brain
15	chr7:102134400-102134800	Enhancers	Fetal Muscle Leg	muscle
16	chr7:102134400-102134800	Active TSS	Thymus	Thymus
17	chr7:102134600-102134800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
18	chr7:102134600-102134800	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr7:102134600-102134800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
20	chr7:102134600-102134800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
21	chr7:102134600-102134800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
22	chr7:102134600-102134800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
23	chr7:102134600-102134800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr7:102134600-102134800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr7:102134600-102134800	Flanking Active TSS	Fetal Thymus	thymus
26	chr7:102134800-102148000	Weak transcription	Fetal Muscle Leg	muscle
27	chr7:102137400-102137600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr7:102137600-102146400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr7:102143000-102143200	Enhancers	Hela-S3	cervix
30	chr7:102143200-102143400	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr7:102143200-102146600	Weak transcription	Hela-S3	cervix
32	chr7:102143600-102153000	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr7:102145200-102145400	Enhancers	Osteobl	bone
34	chr7:102145400-102146400	Weak transcription	Osteobl	bone
35	chr7:102146200-102146600	Enhancers	Skeletal Muscle Male	skeletal muscle
36	chr7:102146200-102146800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr7:102146200-102146800	Enhancers	K562	blood
38	chr7:102146400-102146600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr7:102146400-102146600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr7:102146400-102146800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr7:102146400-102146800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr7:102146400-102146800	Enhancers	NH-A	brain
43	chr7:102146400-102146800	Enhancers	Osteobl	bone
44	chr7:102146600-102147000	Enhancers	Hela-S3	cervix
45	chr7:102146600-102147200	Enhancers	A549	lung
46	chr7:102146600-102147800	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr7:102146600-102149200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr7:102146600-102153000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr7:102146800-102147800	Weak transcription	K562	blood
50	chr7:102146800-102153000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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