Variant report

Variant	esv15614
Chromosome Location	chr7:102113366-102331864
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:7470)
CpG islands
(count:2016)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:7470 , 50 per page) page: 1 2 3 4 5 6 7 ... 150

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	chr7:102254118-102255225	GM12878	blood:	n/a	n/a
9	BATF	chr7:102192870-102193124	GM12878	blood:	n/a	n/a
10	BATF	chr7:102233914-102234227	GM12878	blood:	n/a	n/a
11	BATF	chr7:102205933-102206440	GM12878	blood:	n/a	n/a
12	BATF	chr7:102187719-102187949	GM12878	blood:	n/a	n/a
13	BATF	chr7:102118716-102119971	GM12878	blood:	n/a	n/a
14	BATF	chr7:102313151-102313476	GM12878	blood:	n/a	n/a
15	BATF	chr7:102167226-102167423	GM12878	blood:	n/a	n/a
16	BATF	chr7:102214085-102214343	GM12878	blood:	n/a	n/a
17	BATF	chr7:102120470-102120746	GM12878	blood:	n/a	n/a
18	BATF	chr7:102185674-102186087	GM12878	blood:	n/a	n/a
19	BATF	chr7:102211064-102211322	GM12878	blood:	n/a	n/a
20	BATF	chr7:102329824-102330101	GM12878	blood:	n/a	n/a
21	BATF	chr7:102186680-102187209	GM12878	blood:	n/a	chr7:102186991-102187002
22	BATF	chr7:102155274-102155743	GM12878	blood:	n/a	n/a
23	BATF	chr7:102310144-102310402	GM12878	blood:	n/a	n/a
24	BATF	chr7:102310540-102311004	GM12878	blood:	n/a	n/a
25	BATF	chr7:102305017-102305524	GM12878	blood:	n/a	n/a
26	BATF	chr7:102117804-102118098	GM12878	blood:	n/a	n/a
27	BATF	chr7:102254763-102255038	GM12878	blood:	n/a	n/a
28	BATF	chr7:102135223-102135665	GM12878	blood:	n/a	n/a
29	BATF	chr7:102306478-102306740	GM12878	blood:	n/a	n/a
30	BATF	chr7:102134745-102135058	GM12878	blood:	n/a	n/a
31	BATF	chr7:102152206-102152651	GM12878	blood:	n/a	n/a
32	BATF	chr7:102179720-102179981	GM12878	blood:	n/a	n/a
33	BATF	chr7:102179772-102180041	GM12878	blood:	n/a	n/a
34	BATF	chr7:102312293-102312492	GM12878	blood:	n/a	n/a
35	BATF	chr7:102186661-102187378	GM12878	blood:	n/a	chr7:102186991-102187002
36	BATF	chr7:102251367-102251812	GM12878	blood:	n/a	n/a
37	BATF	chr7:102153892-102154083	GM12878	blood:	n/a	n/a
38	BATF	chr7:102284603-102285287	GM12878	blood:	n/a	n/a
39	BATF	chr7:102211460-102211924	GM12878	blood:	n/a	n/a
40	BATF	chr7:102214079-102214404	GM12878	blood:	n/a	n/a
41	BATF	chr7:102330287-102330744	GM12878	blood:	n/a	n/a
42	BATF	chr7:102291963-102292217	GM12878	blood:	n/a	n/a
43	BATF	chr7:102148082-102148394	GM12878	blood:	n/a	n/a
44	BATF	chr7:102212695-102213163	GM12878	blood:	n/a	n/a
45	BATF	chr7:102285752-102286469	GM12878	blood:	n/a	chr7:102286082-102286093
46	BATF	chr7:102252871-102253062	GM12878	blood:	n/a	n/a
47	BATF	chr7:102266316-102266513	GM12878	blood:	n/a	n/a
48	BATF	chr7:102278880-102279149	GM12878	blood:	n/a	n/a
49	BATF	chr7:102286810-102287040	GM12878	blood:	n/a	n/a
50	BATF	chr7:102207398-102207660	GM12878	blood:	n/a	n/a

(count:2016 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102312308-102312358	AG04449	skin:	fetal
2	chr7:102327236-102327286	HNPCEpiC	eye:	n/a
3	chr7:102119729-102119779	T-47D	breast:	n/a
4	chr7:102312308-102312358	AG04449	skin:	fetal
5	chr7:102327236-102327286	HNPCEpiC	eye:	n/a
6	chr7:102119729-102119779	T-47D	breast:	n/a
7	chr7:102313389-102313439	HPAEpiC	pulmonary alveolar:	n/a
8	chr7:102113759-102113809	Hela-S3	cervix:	n/a
9	chr7:102155527-102155577	T-47D	breast:	n/a
10	chr7:102312200-102312250	HNPCEpiC	eye:	n/a
11	chr7:102132012-102132062	HIPEpiC	eye:	n/a
12	chr7:102279588-102279638	HCPEpiC	choroid plexus:	n/a
13	chr7:102132012-102132062	GM12891	blood:	n/a
14	chr7:102151231-102151281	Hepatocyte	liver:	n/a
15	chr7:102119529-102119579	AG04449	skin:	fetal
16	chr7:102151231-102151281	HRCEpiC	kidney:	n/a
17	chr7:102113759-102113809	SK-N-MC	brain:	n/a
18	chr7:102122352-102122402	PANC-1	pancreas:	n/a
19	chr7:102113508-102113558	H1-hESC	embryonic stem cell:	embryo
20	chr7:102134668-102134718	NHBE	bronchial:	n/a
21	chr7:102155527-102155577	HRPEpiC	eye:	n/a
22	chr7:102312315-102312365	GM12878	blood:	n/a
23	chr7:102279588-102279638	ProgFib	skin:	n/a
24	chr7:102312200-102312250	GM06990	blood:	n/a
25	chr7:102132012-102132062	HNPCEpiC	eye:	n/a
26	chr7:102122352-102122402	MCF-7	breast:	n/a
27	chr7:102312315-102312365	HIPEpiC	eye:	n/a
28	chr7:102136524-102136574	HNPCEpiC	eye:	n/a
29	chr7:102196182-102196232	BJ	skin:	n/a
30	chr7:102259241-102259291	NH-A	brain:	n/a
31	chr7:102279588-102279638	MCF10A-Er-Src	breast:	n/a
32	chr7:102308061-102308111	A549	lung:	n/a
33	chr7:102312318-102312368	HPAEpiC	pulmonary alveolar:	n/a
34	chr7:102312315-102312365	MCF10A-Er-Src	breast:	n/a
35	chr7:102212892-102212942	PrEC	prostate:	n/a
36	chr7:102312308-102312358	T-47D	breast:	n/a
37	chr7:102279588-102279638	MCF-7	breast:	n/a
38	chr7:102327236-102327286	ovcar-3	ovarian:	n/a
39	chr7:102311965-102312015	HCPEpiC	choroid plexus:	n/a
40	chr7:102312200-102312250	Hepatocyte	liver:	n/a
41	chr7:102196182-102196232	AG10803	skin:	n/a
42	chr7:102196182-102196232	PrEC	prostate:	n/a
43	chr7:102119453-102119503	Caco-2	colon:	n/a
44	chr7:102151231-102151281	U87	brain:	n/a
45	chr7:102120464-102120514	HRE	kidney:	n/a
46	chr7:102158209-102158259	GM06990	blood:	n/a
47	chr7:102312315-102312365	AoSMC	blood vessel:	n/a
48	chr7:102151231-102151281	HRPEpiC	eye:	n/a
49	chr7:102134668-102134718	AG09319	gingival:	n/a
50	chr7:102119729-102119779	K562	blood:	n/a

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

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

(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	chr7:102128407-102128431
2	RASA4	hsa-miR-335-5p	chr7:102227581-102227605

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: 2449 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:2449 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147900518	chr7:102113373-102113374	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs200710432	chr7:102113381-102113382	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs369747780	chr7:102113392-102113393	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs549030610	chr7:102113408-102113409	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs191022008	chr7:102113423-102113424	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373015142	chr7:102113433-102113434	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs141694543	chr7:102113451-102113452	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs150396748	chr7:102113452-102113453	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs138157120	chr7:102113460-102113461	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs200957241	chr7:102113472-102113473	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs376230863	chr7:102113473-102113474	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148895778	chr7:102113496-102113497	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs369787035	chr7:102113501-102113502	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs372892312	chr7:102113502-102113503	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376951486	chr7:102113506-102113507	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375482672	chr7:102113508-102113509	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs146938090	chr7:102113509-102113510	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs200399971	chr7:102113514-102113515	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs202157868	chr7:102113520-102113521	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs556142304	chr7:102113528-102113529	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs201620927	chr7:102113530-102113531	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs117004797	chr7:102113554-102113555	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs562725725	chr7:102113555-102113556	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs113355882	chr7:102113559-102113560	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs200797856	chr7:102113563-102113564	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs561274387	chr7:102113564-102113565	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs549304751	chr7:102113565-102113566	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567393178	chr7:102113566-102113567	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs537526506	chr7:102113568-102113569	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs398005638	chr7:102113572-102113573	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs376155179	chr7:102113589-102113590	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs181911821	chr7:102113599-102113600	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs111732861	chr7:102113628-102113629	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs376626887	chr7:102113646-102113647	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs554068315	chr7:102113667-102113668	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs565885423	chr7:102113669-102113670	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs74393036	chr7:102113671-102113672	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs539757267	chr7:102113695-102113696	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs554459534	chr7:102113705-102113706	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs187254105	chr7:102113706-102113707	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs544359221	chr7:102113715-102113716	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs190786714	chr7:102113723-102113724	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs12381	chr7:102113747-102113748	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs545308042	chr7:102113752-102113753	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs112428384	chr7:102113760-102113761	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs576326388	chr7:102113770-102113771	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs527966731	chr7:102113775-102113776	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs543238058	chr7:102113791-102113792	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs73712498	chr7:102113805-102113806	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs376175018	chr7:102113809-102113810	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

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

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	chr7:102106800-102113600	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	chr7:102108400-102113400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr7:102108600-102114600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr7:102108800-102114800	Strong transcription	Brain Germinal Matrix	brain
43	chr7:102109000-102114400	Strong transcription	Esophagus	oesophagus
44	chr7:102109000-102114400	Strong transcription	Fetal Intestine Large	intestine
45	chr7:102109800-102114600	Strong transcription	Right Ventricle	heart
46	chr7:102110000-102114400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr7:102110200-102114200	Strong transcription	Placenta Amnion	Placenta Amnion
48	chr7:102110600-102114400	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr7:102110600-102118200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr7:102110800-102113800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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