Variant report

Variant	nsv471450
Chromosome Location	chr7:102113550-102119381
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr7:102117408-102117666	GM12878	blood:	n/a	n/a
2	BATF	chr7:102118716-102119971	GM12878	blood:	n/a	n/a
3	BATF	chr7:102117804-102118098	GM12878	blood:	n/a	n/a
4	BCL11A	chr7:102118827-102119944	GM12878	blood:	n/a	chr7:102119342-102119355 chr7:102119230-102119243 chr7:102119345-102119354 chr7:102119342-102119351
5	BCL11A	chr7:102117803-102117992	GM12878	blood:	n/a	n/a
6	BCL11A	chr7:102118697-102119525	GM12878	blood:	n/a	chr7:102119342-102119355 chr7:102119230-102119243 chr7:102119345-102119354 chr7:102119342-102119351
7	BCLAF1	chr7:102119230-102119487	GM12878	blood:	n/a	chr7:102119342-102119355 chr7:102119230-102119243 chr7:102119345-102119354 chr7:102119342-102119351
8	BHLHE40	chr7:102119065-102119445	HepG2	liver:	n/a	n/a
9	CBX3	chr7:102118725-102120251	K562	blood:	n/a	n/a
10	CBX3	chr7:102118936-102119564	K562	blood:	n/a	n/a
11	CEBPB	chr7:102118847-102119871	GM12878	blood:	n/a	chr7:102119700-102119712
12	CEBPB	chr7:102118975-102119517	K562	blood:	n/a	n/a
13	CEBPD	chr7:102118987-102119524	K562	blood:	n/a	n/a
14	CTCF	chr7:102119328-102119533	Hela-S3	cervix:	n/a	chr7:102119423-102119441 chr7:102119426-102119436
15	CTCF	chr7:102119300-102119450	GM12871	blood:	n/a	chr7:102119423-102119441 chr7:102119426-102119436
16	CTCF	chr7:102119300-102119450	GM12872	blood:	n/a	chr7:102119423-102119441 chr7:102119426-102119436
17	CTCF	chr7:102119340-102119490	K562	blood:	n/a	chr7:102119423-102119441 chr7:102119426-102119436
18	CTCF	chr7:102119260-102119410	WI-38	lung:	n/a	n/a
19	CTCF	chr7:102119280-102119430	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr7:102119300-102119450	HVMF	connective:	n/a	chr7:102119423-102119441 chr7:102119426-102119436
21	CTCF	chr7:102119280-102119430	HEEpiC	esophagus:	n/a	n/a
22	CTCF	chr7:102119340-102119490	HCPEpiC	choroid plexus:	n/a	chr7:102119423-102119441 chr7:102119426-102119436
23	CTCF	chr7:102119337-102119530	HepG2	liver:	n/a	chr7:102119423-102119441 chr7:102119426-102119436
24	CTCF	chr7:102119300-102119450	HFF	foreskin:	n/a	chr7:102119423-102119441 chr7:102119426-102119436
25	CTCF	chr7:102119280-102119430	HA-sp	spinal cord:	n/a	n/a
26	CTCF	chr7:102119340-102119514	ProgFib	skin:	n/a	chr7:102119423-102119441 chr7:102119426-102119436
27	CTCF	chr7:102119280-102119430	HMF	breast:	n/a	n/a
28	CTCF	chr7:102118963-102119712	A549	lung:	n/a	chr7:102119423-102119441 chr7:102119426-102119436
29	CTCF	chr7:102119312-102119548	GM12892	blood:	n/a	chr7:102119423-102119441 chr7:102119426-102119436
30	CTCF	chr7:102119340-102119490	GM12872	blood:	n/a	chr7:102119423-102119441 chr7:102119426-102119436
31	CTCF	chr7:102119340-102119490	HEK293	kidney:	n/a	chr7:102119423-102119441 chr7:102119426-102119436
32	CTCF	chr7:102119260-102119410	HRE	kidney:	n/a	n/a
33	CTCF	chr7:102119320-102119542	Fibrobl	skin:	n/a	chr7:102119423-102119441 chr7:102119426-102119436
34	CTCF	chr7:102119334-102119559	LNCaP	prostate:	n/a	chr7:102119423-102119441 chr7:102119426-102119436
35	CTCF	chr7:102119280-102119430	GM12873	blood:	n/a	n/a
36	CTCF	chr7:102119306-102119556	GM19238	blood:	n/a	chr7:102119423-102119441 chr7:102119426-102119436
37	CTCF	chr7:102118950-102119929	A549	lung:	n/a	chr7:102119423-102119441 chr7:102119730-102119743 chr7:102119426-102119436
38	CTCF	chr7:102119300-102119450	HFF-Myc	foreskin:	n/a	chr7:102119423-102119441 chr7:102119426-102119436
39	CTCF	chr7:102119340-102119490	SAEC	small airway:	n/a	chr7:102119423-102119441 chr7:102119426-102119436
40	CTCF	chr7:102119176-102119560	A549	lung:	n/a	chr7:102119423-102119441 chr7:102119426-102119436
41	CTCF	chr7:102119300-102119450	GM12873	blood:	n/a	chr7:102119423-102119441 chr7:102119426-102119436
42	CTCF	chr7:102119280-102119430	GM12878	blood:	n/a	n/a
43	CTCF	chr7:102119232-102119599	K562	blood:	n/a	chr7:102119423-102119441 chr7:102119426-102119436
44	CTCF	chr7:102119305-102119487	SK-N-SH_RA	brain:	n/a	chr7:102119423-102119441 chr7:102119426-102119436
45	CTCF	chr7:102115391-102115487	Gliobla	brain:	n/a	n/a
46	CTCF	chr7:102119308-102119554	GM19239	blood:	n/a	chr7:102119423-102119441 chr7:102119426-102119436
47	CTCF	chr7:102119261-102119489	A549	lung:	n/a	chr7:102119423-102119441 chr7:102119426-102119436
48	CTCF	chr7:102119236-102119480	H1-hESC	embryonic stem cell:	n/a	chr7:102119423-102119441 chr7:102119426-102119436
49	CTCF	chr7:102119304-102119499	H1-hESC	embryonic stem cell:	n/a	chr7:102119423-102119441 chr7:102119426-102119436
50	CTCF	chr7:102119296-102119499	SK-N-SH_RA	brain:	n/a	chr7:102119423-102119441 chr7:102119426-102119436

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102113508-102113558	T-47D	breast:	n/a
2	chr7:102118300-102118350	PFSK-1	brain:	n/a
3	chr7:102113759-102113809	PFSK-1	brain:	n/a
4	chr7:102113508-102113558	GM12878	blood:	n/a
5	chr7:102118300-102118350	LNCaP	prostate:	n/a
6	chr7:102118300-102118350	NHBE	bronchial:	n/a
7	chr7:102113759-102113809	Jurkat	blood:	n/a
8	chr7:102113759-102113809	AoSMC	blood vessel:	n/a
9	chr7:102113508-102113558	BJ	skin:	n/a
10	chr7:102113759-102113809	BE2_C	brain:	n/a
11	chr7:102113759-102113809	HRPEpiC	eye:	n/a
12	chr7:102118300-102118350	HNPCEpiC	eye:	n/a
13	chr7:102113759-102113809	NB4	blood:	n/a
14	chr7:102113759-102113809	NT2-D1	testis:	n/a
15	chr7:102113508-102113558	NT2-D1	testis:	n/a
16	chr7:102118300-102118350	HEEpiC	esophagus:	n/a
17	chr7:102113508-102113558	HRE	kidney:	n/a
18	chr7:102113759-102113809	HL-60	blood:	n/a
19	chr7:102113508-102113558	GM12891	blood:	n/a
20	chr7:102118300-102118350	GM12878	blood:	n/a
21	chr7:102113508-102113558	AG04449	skin:	fetal
22	chr7:102118300-102118350	ovcar-3	ovarian:	n/a
23	chr7:102113759-102113809	T-47D	breast:	n/a
24	chr7:102113508-102113558	ProgFib	skin:	n/a
25	chr7:102113759-102113809	A549	lung:	n/a
26	chr7:102113508-102113558	NHDF-neo	bronchial:	n/a
27	chr7:102118300-102118350	PrEC	prostate:	n/a
28	chr7:102113508-102113558	HMEC	breast:	n/a
29	chr7:102113508-102113558	HCM	heart:	n/a
30	chr7:102113508-102113558	GM12892	blood:	n/a
31	chr7:102113759-102113809	HEK293	kidney:	embryo
32	chr7:102113508-102113558	U87	brain:	n/a
33	chr7:102113508-102113558	GM19239	blood:	n/a
34	chr7:102118300-102118350	HMEC	breast:	n/a
35	chr7:102113759-102113809	SK-N-SH	brain:	n/a
36	chr7:102113759-102113809	HNPCEpiC	eye:	n/a
37	chr7:102118300-102118350	HIPEpiC	eye:	n/a
38	chr7:102113759-102113809	NHBE	bronchial:	n/a
39	chr7:102113759-102113809	HUVEC	blood vessel:	n/a
40	chr7:102113759-102113809	Caco-2	colon:	n/a
41	chr7:102113759-102113809	CMK	blood:	n/a
42	chr7:102118300-102118350	GM12892	blood:	n/a
43	chr7:102113759-102113809	RPTEC	kidney:	n/a
44	chr7:102113508-102113558	IMR90	lung:	fetal
45	chr7:102118300-102118350	HEK293	kidney:	embryo
46	chr7:102118300-102118350	HAEpiC	amniotic membrane:	n/a
47	chr7:102118300-102118350	ECC-1	luminal epithelium:	n/a
48	chr7:102118300-102118350	MCF-7	breast:	n/a
49	chr7:102113759-102113809	GM06990	blood:	n/a
50	chr7:102113759-102113809	HAEpiC	amniotic membrane:	n/a

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:

Variant related genes	Relation type
ENSG00000271745	TF binding region
POLR2J	TF binding region
ENSG00000271745	CpG island
POLR2J	CpG island
ENSG00000264471	chromatin interactions

Extended variants
information (count: 285 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:285 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117004797	chr7:102113554-102113555	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs562725725	chr7:102113555-102113556	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs113355882	chr7:102113559-102113560	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs200797856	chr7:102113563-102113564	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs561274387	chr7:102113564-102113565	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs549304751	chr7:102113565-102113566	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs567393178	chr7:102113566-102113567	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs537526506	chr7:102113568-102113569	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs398005638	chr7:102113572-102113573	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs376155179	chr7:102113589-102113590	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs181911821	chr7:102113599-102113600	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs111732861	chr7:102113628-102113629	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs376626887	chr7:102113646-102113647	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs554068315	chr7:102113667-102113668	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565885423	chr7:102113669-102113670	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs74393036	chr7:102113671-102113672	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs539757267	chr7:102113695-102113696	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs554459534	chr7:102113705-102113706	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs187254105	chr7:102113706-102113707	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs544359221	chr7:102113715-102113716	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs190786714	chr7:102113723-102113724	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs12381	chr7:102113747-102113748	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs545308042	chr7:102113752-102113753	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs112428384	chr7:102113760-102113761	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs576326388	chr7:102113770-102113771	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527966731	chr7:102113775-102113776	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs543238058	chr7:102113791-102113792	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73712498	chr7:102113805-102113806	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs376175018	chr7:102113809-102113810	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531457132	chr7:102113833-102113834	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs182636699	chr7:102113835-102113836	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs1131384	chr7:102113841-102113842	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs532097506	chr7:102113845-102113846	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs112519829	chr7:102113872-102113873	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs376986914	chr7:102113882-102113883	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566019847	chr7:102113890-102113891	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs141766635	chr7:102113891-102113892	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs532211452	chr7:102113895-102113896	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs369918493	chr7:102113896-102113897	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs201743245	chr7:102113897-102113898	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554777490	chr7:102113898-102113899	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs4552831	chr7:102113899-102113900	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs569725557	chr7:102113902-102113903	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs538354253	chr7:102113903-102113904	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs1131383	chr7:102113909-102113910	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs577620128	chr7:102113911-102113912	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs188146786	chr7:102113912-102113913	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs149032417	chr7:102113915-102113916	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs553731044	chr7:102113916-102113917	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs375322024	chr7:102113920-102113921	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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

Chromatin state (count:394 , 50 per page) page: 1 2 3 4 5 6 7 8

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	chr7:102106800-102113600	Weak transcription	Colon Smooth Muscle	Colon
5	chr7:102106800-102113600	Weak transcription	Hela-S3	cervix
6	chr7:102106800-102114400	Weak transcription	Brain Angular Gyrus	brain
7	chr7:102106800-102114400	Strong transcription	NHLF	lung
8	chr7:102106800-102114600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr7:102106800-102114600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr7:102106800-102116400	Strong transcription	Fetal Stomach	stomach
11	chr7:102106800-102118800	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr7:102106800-102119200	Weak transcription	NHDF-Ad	bronchial
13	chr7:102107400-102116200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr7:102107400-102116200	Strong transcription	Primary neutrophils fromperipheralblood	blood
15	chr7:102107600-102118200	Weak transcription	HUVEC	blood vessel
16	chr7:102107600-102119200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr7:102107600-102120400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr7:102107800-102114200	Weak transcription	Fetal Brain Male	brain
19	chr7:102107800-102114400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
20	chr7:102107800-102114400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr7:102107800-102114600	Strong transcription	Primary B cells from peripheral blood	blood
22	chr7:102107800-102114600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr7:102107800-102114800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr7:102107800-102115600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
25	chr7:102107800-102116000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr7:102107800-102116400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr7:102107800-102118000	Weak transcription	NH-A	brain
28	chr7:102108000-102113600	Strong transcription	Cortex derived primary cultured neurospheres	brain
29	chr7:102108000-102113800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr7:102108000-102114600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr7:102108000-102114600	Strong transcription	HUES6 Cell Line	embryonic stem cell
32	chr7:102108000-102114600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr7:102108000-102114600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr7:102108000-102114600	Strong transcription	Fetal Brain Female	brain
35	chr7:102108000-102114800	Strong transcription	Thymus	Thymus
36	chr7:102108000-102115000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
37	chr7:102108000-102115400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
38	chr7:102108000-102115600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr7:102108200-102115000	Strong transcription	Fetal Thymus	thymus
40	chr7:102108600-102114600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr7:102108800-102114800	Strong transcription	Brain Germinal Matrix	brain
42	chr7:102109000-102114400	Strong transcription	Esophagus	oesophagus
43	chr7:102109000-102114400	Strong transcription	Fetal Intestine Large	intestine
44	chr7:102109800-102114600	Strong transcription	Right Ventricle	heart
45	chr7:102110000-102114400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr7:102110200-102114200	Strong transcription	Placenta Amnion	Placenta Amnion
47	chr7:102110600-102114400	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr7:102110600-102118200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr7:102110800-102113800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr7:102111000-102114800	Strong transcription	Gastric	stomach

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