Variant report

Variant	nsv888844
Chromosome Location	chr7:102113909-102352629
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:7514)
CpG islands
(count:1954)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:7514 , 50 per page) page: 1 2 3 4 5 6 7 ... 151

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102339769-102340073	K562	blood:	n/a	n/a
2	ARID3A	chr7:102212897-102213097	HepG2	liver:	n/a	n/a
3	ATF1	chr7:102339824-102340183	K562	blood:	n/a	n/a
4	ATF2	chr7:102153014-102153393	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr7:102312022-102312401	A549	lung:	n/a	chr7:102312144-102312152
6	ATF3	chr7:102213014-102213188	K562	blood:	n/a	n/a
7	ATF3	chr7:102213014-102213141	GM12878	blood:	n/a	n/a
8	ATF3	chr7:102312099-102312242	K562	blood:	n/a	chr7:102312144-102312152
9	BACH1	chr7:102213021-102213172	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr7:102247244-102247556	GM12878	blood:	n/a	n/a
11	BATF	chr7:102167226-102167423	GM12878	blood:	n/a	n/a
12	BATF	chr7:102212695-102213163	GM12878	blood:	n/a	n/a
13	BATF	chr7:102155274-102155743	GM12878	blood:	n/a	n/a
14	BATF	chr7:102134745-102135058	GM12878	blood:	n/a	n/a
15	BATF	chr7:102185510-102186196	GM12878	blood:	n/a	n/a
16	BATF	chr7:102310144-102310402	GM12878	blood:	n/a	n/a
17	BATF	chr7:102329824-102330101	GM12878	blood:	n/a	n/a
18	BATF	chr7:102285752-102286469	GM12878	blood:	n/a	chr7:102286082-102286093
19	BATF	chr7:102313180-102313439	GM12878	blood:	n/a	n/a
20	BATF	chr7:102352581-102352892	GM12878	blood:	n/a	n/a
21	BATF	chr7:102211064-102211322	GM12878	blood:	n/a	n/a
22	BATF	chr7:102185674-102186087	GM12878	blood:	n/a	n/a
23	BATF	chr7:102266316-102266513	GM12878	blood:	n/a	n/a
24	BATF	chr7:102234392-102234834	GM12878	blood:	n/a	n/a
25	BATF	chr7:102158383-102158641	GM12878	blood:	n/a	n/a
26	BATF	chr7:102192870-102193124	GM12878	blood:	n/a	n/a
27	BATF	chr7:102284765-102285178	GM12878	blood:	n/a	n/a
28	BATF	chr7:102310540-102311004	GM12878	blood:	n/a	n/a
29	BATF	chr7:102205933-102206440	GM12878	blood:	n/a	n/a
30	BATF	chr7:102155139-102156246	GM12878	blood:	n/a	n/a
31	BATF	chr7:102186680-102187209	GM12878	blood:	n/a	chr7:102186991-102187002
32	BATF	chr7:102117804-102118098	GM12878	blood:	n/a	n/a
33	BATF	chr7:102186661-102187378	GM12878	blood:	n/a	chr7:102186991-102187002
34	BATF	chr7:102254118-102255225	GM12878	blood:	n/a	n/a
35	BATF	chr7:102293584-102293766	GM12878	blood:	n/a	n/a
36	BATF	chr7:102256202-102256653	GM12878	blood:	n/a	n/a
37	BATF	chr7:102157223-102157674	GM12878	blood:	n/a	n/a
38	BATF	chr7:102285771-102286300	GM12878	blood:	n/a	chr7:102286082-102286093
39	BATF	chr7:102257362-102257620	GM12878	blood:	n/a	n/a
40	BATF	chr7:102286810-102287040	GM12878	blood:	n/a	n/a
41	BATF	chr7:102252871-102253062	GM12878	blood:	n/a	n/a
42	BATF	chr7:102179720-102179981	GM12878	blood:	n/a	n/a
43	BATF	chr7:102306478-102306740	GM12878	blood:	n/a	n/a
44	BATF	chr7:102212379-102213628	GM12878	blood:	n/a	n/a
45	BATF	chr7:102291963-102292217	GM12878	blood:	n/a	n/a
46	BATF	chr7:102284603-102285287	GM12878	blood:	n/a	n/a
47	BATF	chr7:102254253-102254722	GM12878	blood:	n/a	n/a
48	BATF	chr7:102312293-102312492	GM12878	blood:	n/a	n/a
49	BATF	chr7:102211460-102211924	GM12878	blood:	n/a	n/a
50	BATF	chr7:102313151-102313476	GM12878	blood:	n/a	n/a

(count:1954 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102312200-102312250	PANC-1	pancreas:	n/a
2	chr7:102155527-102155577	NH-A	brain:	n/a
3	chr7:102312200-102312250	PANC-1	pancreas:	n/a
4	chr7:102155527-102155577	NH-A	brain:	n/a
5	chr7:102132012-102132062	AG04450	lung:	fetal
6	chr7:102151231-102151281	HCM	heart:	n/a
7	chr7:102151231-102151281	NT2-D1	testis:	n/a
8	chr7:102120464-102120514	HMEC	breast:	n/a
9	chr7:102312318-102312368	NT2-D1	testis:	n/a
10	chr7:102313412-102313462	AG09309	skin:	n/a
11	chr7:102327236-102327286	SKMC	muscle:	n/a
12	chr7:102312200-102312250	T-47D	breast:	n/a
13	chr7:102312318-102312368	HNPCEpiC	eye:	n/a
14	chr7:102122352-102122402	SKMC	muscle:	n/a
15	chr7:102119529-102119579	HAEpiC	amniotic membrane:	n/a
16	chr7:102119710-102119760	MCF-7	breast:	n/a
17	chr7:102155527-102155577	HRCEpiC	kidney:	n/a
18	chr7:102308061-102308111	HL-60	blood:	n/a
19	chr7:102327236-102327286	HCF	heart:	n/a
20	chr7:102118300-102118350	SK-N-SH	brain:	n/a
21	chr7:102312315-102312365	HMEC	breast:	n/a
22	chr7:102313389-102313439	HMEC	breast:	n/a
23	chr7:102120464-102120514	SK-N-SH	brain:	n/a
24	chr7:102161506-102161556	ProgFib	skin:	n/a
25	chr7:102246378-102246428	GM06990	blood:	n/a
26	chr7:102312318-102312368	AG09309	skin:	n/a
27	chr7:102132012-102132062	T-47D	breast:	n/a
28	chr7:102312331-102312381	RPTEC	kidney:	n/a
29	chr7:102120464-102120514	BJ	skin:	n/a
30	chr7:102313412-102313462	HRPEpiC	eye:	n/a
31	chr7:102312308-102312358	A549	lung:	n/a
32	chr7:102119453-102119503	Hepatocyte	liver:	n/a
33	chr7:102313412-102313462	HEK293	kidney:	embryo
34	chr7:102279588-102279638	HNPCEpiC	eye:	n/a
35	chr7:102312308-102312358	Caco-2	colon:	n/a
36	chr7:102122352-102122402	LNCaP	prostate:	n/a
37	chr7:102313412-102313462	HEEpiC	esophagus:	n/a
38	chr7:102132012-102132062	Jurkat	blood:	n/a
39	chr7:102158209-102158259	LNCaP	prostate:	n/a
40	chr7:102136524-102136574	NHDF-neo	bronchial:	n/a
41	chr7:102119729-102119779	SAEC	small airway:	n/a
42	chr7:102118300-102118350	Hela-S3	cervix:	n/a
43	chr7:102332458-102332508	HCM	heart:	n/a
44	chr7:102134668-102134718	HRCEpiC	kidney:	n/a
45	chr7:102246378-102246428	GM12891	blood:	n/a
46	chr7:102246378-102246428	IMR90	lung:	fetal
47	chr7:102329146-102329196	T-47D	breast:	n/a
48	chr7:102312318-102312368	GM19239	blood:	n/a
49	chr7:102330635-102330685	HRCEpiC	kidney:	n/a
50	chr7:102312318-102312368	HUVEC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:102095105..102097142-chr7:102112791..102114354,2	K562	blood:
2	chr7:102110592..102113197-chr7:102117853..102119354,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POLR2J-1	chr7:102120179-102121095	NONHSAT122510

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
RASA4B	TF binding region
ENSG00000272949	TF binding region
ENSG00000205236	TF binding region
POLR2J	TF binding region
ENSG00000228049	TF binding region
ENSG00000238997	TF binding region
UPK3BL	TF binding region
POLR2J2	TF binding region
SPDYE2	TF binding region
ENSG00000271745	TF binding region
RASA4	TF binding region
RASA4DP	TF binding region
POLR2J3	TF binding region
SPDYE2B	TF binding region
ENSG00000256604	TF binding region
ENSG00000238392	TF binding region
ENSG00000270249	CpG island
RASA4B	CpG island
ENSG00000272949	CpG island
ENSG00000205236	CpG island
POLR2J	CpG island
ENSG00000228049	CpG island
ENSG00000238997	CpG island
UPK3BL	CpG island
POLR2J2	CpG island
SPDYE2	CpG island
ENSG00000271745	CpG island
RASA4	CpG island
RASA4DP	CpG island
POLR2J3	CpG island
SPDYE2B	CpG island
ENSG00000256604	CpG island
ENSG00000238392	CpG island
ENSG00000264471	chromatin interactions

Extended variants
information (count: 2714 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:2714 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1131383	chr7:102113909-102113910	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs577620128	chr7:102113911-102113912	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs188146786	chr7:102113912-102113913	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149032417	chr7:102113915-102113916	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs553731044	chr7:102113916-102113917	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs375322024	chr7:102113920-102113921	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs374647577	chr7:102113930-102113931	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572431573	chr7:102113945-102113946	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs576255328	chr7:102113973-102113974	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs145098202	chr7:102113982-102113983	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs374754131	chr7:102113983-102113984	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs542922406	chr7:102113995-102113996	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs7950	chr7:102114006-102114007	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs531771531	chr7:102114007-102114008	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs543506379	chr7:102114010-102114011	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs565020710	chr7:102114011-102114012	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532236085	chr7:102114014-102114015	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs547451689	chr7:102114020-102114021	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs560568271	chr7:102114025-102114026	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs79690771	chr7:102114026-102114027	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs530025714	chr7:102114036-102114037	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs150167848	chr7:102114037-102114038	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs138572994	chr7:102114050-102114051	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs551941302	chr7:102114054-102114055	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs368315599	chr7:102114064-102114065	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs141765538	chr7:102114074-102114075	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs2229797	chr7:102114075-102114076	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs190239304	chr7:102114080-102114081	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs2229796	chr7:102114087-102114088	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs1131359	chr7:102114090-102114091	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs146329268	chr7:102114093-102114094	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs372295917	chr7:102114096-102114097	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs200998035	chr7:102114103-102114104	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs369643503	chr7:102114144-102114145	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs375875273	chr7:102114145-102114146	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs139640335	chr7:102114148-102114149	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs75106520	chr7:102114151-102114152	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs369471371	chr7:102114152-102114153	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs372453110	chr7:102114155-102114156	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs565463742	chr7:102114158-102114159	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs377030778	chr7:102114159-102114160	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs370759626	chr7:102114164-102114165	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs373619328	chr7:102114173-102114174	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs34036426	chr7:102114179-102114180	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577042524	chr7:102114198-102114199	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs576314969	chr7:102114206-102114207	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs541100454	chr7:102114207-102114208	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs559409345	chr7:102114210-102114211	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs529620182	chr7:102114211-102114212	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548471539	chr7:102114212-102114213	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
early-passage human iPS cells	21368824	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
Ovarian cancer	21781307	CNVD

Chromatin state (count:1437 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102106400-102119400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr7:102106600-102115000	Weak transcription	Primary hematopoietic stem cells	blood
3	chr7:102106600-102119200	Weak transcription	Right Atrium	heart
4	chr7:102106800-102114400	Weak transcription	Brain Angular Gyrus	brain
5	chr7:102106800-102114400	Strong transcription	NHLF	lung
6	chr7:102106800-102114600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr7:102106800-102114600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr7:102106800-102116400	Strong transcription	Fetal Stomach	stomach
9	chr7:102106800-102118800	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr7:102106800-102119200	Weak transcription	NHDF-Ad	bronchial
11	chr7:102107400-102116200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr7:102107400-102116200	Strong transcription	Primary neutrophils fromperipheralblood	blood
13	chr7:102107600-102118200	Weak transcription	HUVEC	blood vessel
14	chr7:102107600-102119200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr7:102107600-102120400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr7:102107800-102114200	Weak transcription	Fetal Brain Male	brain
17	chr7:102107800-102114400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
18	chr7:102107800-102114400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr7:102107800-102114600	Strong transcription	Primary B cells from peripheral blood	blood
20	chr7:102107800-102114600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr7:102107800-102114800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr7:102107800-102115600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr7:102107800-102116000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr7:102107800-102116400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr7:102107800-102118000	Weak transcription	NH-A	brain
26	chr7:102108000-102114600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr7:102108000-102114600	Strong transcription	HUES6 Cell Line	embryonic stem cell
28	chr7:102108000-102114600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr7:102108000-102114600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr7:102108000-102114600	Strong transcription	Fetal Brain Female	brain
31	chr7:102108000-102114800	Strong transcription	Thymus	Thymus
32	chr7:102108000-102115000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
33	chr7:102108000-102115400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
34	chr7:102108000-102115600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr7:102108200-102115000	Strong transcription	Fetal Thymus	thymus
36	chr7:102108600-102114600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr7:102108800-102114800	Strong transcription	Brain Germinal Matrix	brain
38	chr7:102109000-102114400	Strong transcription	Esophagus	oesophagus
39	chr7:102109000-102114400	Strong transcription	Fetal Intestine Large	intestine
40	chr7:102109800-102114600	Strong transcription	Right Ventricle	heart
41	chr7:102110000-102114400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr7:102110200-102114200	Strong transcription	Placenta Amnion	Placenta Amnion
43	chr7:102110600-102114400	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr7:102110600-102118200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr7:102111000-102114800	Strong transcription	Gastric	stomach
46	chr7:102111000-102114800	Strong transcription	Spleen	Spleen
47	chr7:102111000-102116400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr7:102111000-102116400	Strong transcription	Fetal Intestine Small	intestine
49	chr7:102111600-102114000	Strong transcription	HUES64 Cell Line	embryonic stem cell
50	chr7:102111600-102114600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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