Variant report

Variant	nsv608054
Chromosome Location	chr7:102256656-102359715
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2734)
CpG islands
(count:916)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2734 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

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	ATF1	chr7:102339824-102340183	K562	blood:	n/a	n/a
3	ATF2	chr7:102353660-102354116	GM12878	blood:	n/a	n/a
4	ATF2	chr7:102353714-102354151	GM12878	blood:	n/a	n/a
5	ATF3	chr7:102312022-102312401	A549	lung:	n/a	chr7:102312144-102312152
6	ATF3	chr7:102312099-102312242	K562	blood:	n/a	chr7:102312144-102312152
7	BATF	chr7:102284765-102285178	GM12878	blood:	n/a	n/a
8	BATF	chr7:102330287-102330744	GM12878	blood:	n/a	n/a
9	BATF	chr7:102352581-102352892	GM12878	blood:	n/a	n/a
10	BATF	chr7:102313180-102313439	GM12878	blood:	n/a	n/a
11	BATF	chr7:102257362-102257620	GM12878	blood:	n/a	n/a
12	BATF	chr7:102278828-102279089	GM12878	blood:	n/a	n/a
13	BATF	chr7:102286810-102287040	GM12878	blood:	n/a	n/a
14	BATF	chr7:102306478-102306740	GM12878	blood:	n/a	n/a
15	BATF	chr7:102313151-102313476	GM12878	blood:	n/a	n/a
16	BATF	chr7:102311459-102312701	GM12878	blood:	n/a	n/a
17	BATF	chr7:102266316-102266513	GM12878	blood:	n/a	n/a
18	BATF	chr7:102352630-102352884	GM12878	blood:	n/a	n/a
19	BATF	chr7:102285771-102286300	GM12878	blood:	n/a	chr7:102286082-102286093
20	BATF	chr7:102284603-102285287	GM12878	blood:	n/a	n/a
21	BATF	chr7:102291963-102292217	GM12878	blood:	n/a	n/a
22	BATF	chr7:102310540-102311004	GM12878	blood:	n/a	n/a
23	BATF	chr7:102353721-102354553	GM12878	blood:	n/a	n/a
24	BATF	chr7:102355536-102355847	GM12878	blood:	n/a	n/a
25	BATF	chr7:102312293-102312492	GM12878	blood:	n/a	n/a
26	BATF	chr7:102329824-102330101	GM12878	blood:	n/a	n/a
27	BATF	chr7:102305017-102305524	GM12878	blood:	n/a	n/a
28	BATF	chr7:102278880-102279149	GM12878	blood:	n/a	n/a
29	BATF	chr7:102356109-102356632	GM12878	blood:	n/a	n/a
30	BATF	chr7:102355431-102355796	GM12878	blood:	n/a	n/a
31	BATF	chr7:102310144-102310402	GM12878	blood:	n/a	n/a
32	BATF	chr7:102353557-102354555	GM12878	blood:	n/a	n/a
33	BATF	chr7:102285752-102286469	GM12878	blood:	n/a	chr7:102286082-102286093
34	BATF	chr7:102356182-102356563	GM12878	blood:	n/a	n/a
35	BATF	chr7:102293584-102293766	GM12878	blood:	n/a	n/a
36	BCL11A	chr7:102285737-102286323	GM12878	blood:	n/a	n/a
37	BCL11A	chr7:102312275-102312544	GM12878	blood:	n/a	chr7:102312277-102312290
38	BCL11A	chr7:102278940-102279146	GM12878	blood:	n/a	n/a
39	BCL11A	chr7:102353677-102354018	GM12878	blood:	n/a	n/a
40	BCL11A	chr7:102283861-102284058	GM12878	blood:	n/a	n/a
41	BCL11A	chr7:102306449-102306783	GM12878	blood:	n/a	n/a
42	BCL11A	chr7:102305225-102305593	GM12878	blood:	n/a	chr7:102305424-102305433
43	BCL11A	chr7:102284155-102284333	GM12878	blood:	n/a	n/a
44	BCL11A	chr7:102296701-102296848	GM12878	blood:	n/a	n/a
45	BCL11A	chr7:102330382-102330951	GM12878	blood:	n/a	chr7:102330751-102330764
46	BCL11A	chr7:102352667-102352857	GM12878	blood:	n/a	n/a
47	BCL11A	chr7:102278790-102279352	GM12878	blood:	n/a	n/a
48	BCL11A	chr7:102301836-102301994	GM12878	blood:	n/a	n/a
49	BCL11A	chr7:102353630-102354526	GM12878	blood:	n/a	n/a
50	BCL11A	chr7:102329229-102329596	GM12878	blood:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102312308-102312358	CMK	blood:	n/a
2	chr7:102312308-102312358	CMK	blood:	n/a
3	chr7:102327236-102327286	NHBE	bronchial:	n/a
4	chr7:102259241-102259291	NH-A	brain:	n/a
5	chr7:102312318-102312368	BJ	skin:	n/a
6	chr7:102279588-102279638	AG09319	gingival:	n/a
7	chr7:102312315-102312365	Caco-2	colon:	n/a
8	chr7:102313389-102313439	LNCaP	prostate:	n/a
9	chr7:102279588-102279638	AG04450	lung:	fetal
10	chr7:102329146-102329196	HRCEpiC	kidney:	n/a
11	chr7:102313412-102313462	HNPCEpiC	eye:	n/a
12	chr7:102312308-102312358	MCF-7	breast:	n/a
13	chr7:102327236-102327286	RPTEC	kidney:	n/a
14	chr7:102332458-102332508	SAEC	small airway:	n/a
15	chr7:102312318-102312368	MCF-7	breast:	n/a
16	chr7:102312200-102312250	HNPCEpiC	eye:	n/a
17	chr7:102327236-102327286	AoSMC	blood vessel:	n/a
18	chr7:102329146-102329196	PrEC	prostate:	n/a
19	chr7:102312200-102312250	AoSMC	blood vessel:	n/a
20	chr7:102312331-102312381	PANC-1	pancreas:	n/a
21	chr7:102311965-102312015	Caco-2	colon:	n/a
22	chr7:102312315-102312365	AG09319	gingival:	n/a
23	chr7:102313389-102313439	AG04449	skin:	fetal
24	chr7:102313389-102313439	GM12878	blood:	n/a
25	chr7:102312315-102312365	HL-60	blood:	n/a
26	chr7:102327236-102327286	HEK293	kidney:	embryo
27	chr7:102259241-102259291	NB4	blood:	n/a
28	chr7:102259241-102259291	HIPEpiC	eye:	n/a
29	chr7:102312331-102312381	ProgFib	skin:	n/a
30	chr7:102312200-102312250	SK-N-MC	brain:	n/a
31	chr7:102313412-102313462	RPTEC	kidney:	n/a
32	chr7:102313412-102313462	HRE	kidney:	n/a
33	chr7:102308061-102308111	GM12891	blood:	n/a
34	chr7:102312308-102312358	GM12892	blood:	n/a
35	chr7:102327236-102327286	SAEC	small airway:	n/a
36	chr7:102311965-102312015	T-47D	breast:	n/a
37	chr7:102332458-102332508	PrEC	prostate:	n/a
38	chr7:102311965-102312015	SK-N-SH_RA	brain:	n/a
39	chr7:102312331-102312381	AG09309	skin:	n/a
40	chr7:102308061-102308111	HL-60	blood:	n/a
41	chr7:102312331-102312381	HMEC	breast:	n/a
42	chr7:102279588-102279638	MCF10A-Er-Src	breast:	n/a
43	chr7:102308061-102308111	ovcar-3	ovarian:	n/a
44	chr7:102279588-102279638	BE2_C	brain:	n/a
45	chr7:102332458-102332508	AG09309	skin:	n/a
46	chr7:102327236-102327286	HRCEpiC	kidney:	n/a
47	chr7:102312331-102312381	SK-N-SH_RA	brain:	n/a
48	chr7:102312315-102312365	LNCaP	prostate:	n/a
49	chr7:102312331-102312381	NHBE	bronchial:	n/a
50	chr7:102313412-102313462	HIPEpiC	eye:	n/a

No data

Variant related genes	Relation type
ENSG00000205236	TF binding region
ENSG00000228049	TF binding region
UPK3BL	TF binding region
POLR2J2	TF binding region
RASA4	TF binding region
RASA4DP	TF binding region
SPDYE2B	TF binding region
ENSG00000205236	CpG island
ENSG00000228049	CpG island
UPK3BL	CpG island
POLR2J2	CpG island
RASA4	CpG island
RASA4DP	CpG island
SPDYE2B	CpG island

Extended variants
information (count: 1353 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1353 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370288140	chr7:102257022-102257023	Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs150204185	chr7:102257116-102257117	Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs146516658	chr7:102257124-102257125	Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs533929081	chr7:102257150-102257151	Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs374409068	chr7:102257171-102257172	Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs549695260	chr7:102257175-102257176	Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs376878121	chr7:102257177-102257178	Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs567840845	chr7:102257615-102257616	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs538464357	chr7:102257775-102257776	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs376559402	chr7:102257830-102257831	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs7384540	chr7:102257833-102257834	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs7384555	chr7:102257851-102257852	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs375602761	chr7:102258012-102258013	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs373611909	chr7:102258048-102258049	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs148558097	chr7:102258158-102258159	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs144036743	chr7:102258227-102258228	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs143001111	chr7:102258528-102258529	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs373696061	chr7:102258572-102258573	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs556759169	chr7:102258696-102258697	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs111563401	chr7:102258720-102258721	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs113656318	chr7:102258721-102258722	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs71213106	chr7:102258794-102258795	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs577833133	chr7:102258799-102258800	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs7793553	chr7:102258800-102258801	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs369254427	chr7:102258801-102258802	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs572118569	chr7:102258856-102258857	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs373360161	chr7:102258974-102258975	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs28578541	chr7:102259002-102259003	Genic enhancers Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
29	rs377672963	chr7:102259063-102259064	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542237271	chr7:102259203-102259204	Genic enhancers Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs561272038	chr7:102259247-102259248	Genic enhancers Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs576342878	chr7:102259261-102259262	Genic enhancers Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs377526555	chr7:102259280-102259281	Genic enhancers Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs543626347	chr7:102259298-102259299	Genic enhancers Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs564692913	chr7:102259302-102259303	Genic enhancers Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs533262928	chr7:102259329-102259330	Genic enhancers Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs551502567	chr7:102259417-102259418	Genic enhancers Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs577432970	chr7:102259461-102259462	Genic enhancers Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs560207335	chr7:102259485-102259486	Genic enhancers Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs371371576	chr7:102259507-102259508	Genic enhancers Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs527710576	chr7:102259560-102259561	Genic enhancers Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs549091715	chr7:102259585-102259586	Genic enhancers Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs370246699	chr7:102259615-102259616	Genic enhancers Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs371025274	chr7:102259639-102259640	Genic enhancers Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs12535818	chr7:102259672-102259673	Genic enhancers Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs373565072	chr7:102259678-102259679	Genic enhancers Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs56267042	chr7:102259727-102259728	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs112745904	chr7:102259794-102259795	Genic enhancers Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs567962601	chr7:102259883-102259884	Genic enhancers Enhancers ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs111664704	chr7:102259887-102259888	Genic enhancers Enhancers ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	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
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:361 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102252600-102257600	Weak transcription	Brain Angular Gyrus	brain
2	chr7:102252800-102257000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:102252800-102257000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr7:102252800-102257000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr7:102252800-102257000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr7:102252800-102257000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr7:102252800-102257000	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr7:102252800-102257000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr7:102252800-102257000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr7:102252800-102257000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr7:102252800-102257000	Weak transcription	Brain Anterior Caudate	brain
12	chr7:102252800-102257000	Weak transcription	Brain Germinal Matrix	brain
13	chr7:102252800-102257000	Weak transcription	Colonic Mucosa	Colon
14	chr7:102252800-102257000	Weak transcription	Dnd41	blood
15	chr7:102252800-102257000	Weak transcription	HUVEC	blood vessel
16	chr7:102252800-102257000	Weak transcription	K562	blood
17	chr7:102252800-102257400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
18	chr7:102252800-102257600	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr7:102252800-102257800	Weak transcription	Brain Substantia Nigra	brain
20	chr7:102254600-102257000	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr7:102254600-102257000	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr7:102254600-102257000	Weak transcription	Primary B cells from cord blood	blood
23	chr7:102254600-102257000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr7:102254600-102257000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr7:102254600-102257000	Weak transcription	Adipose Nuclei	Adipose
26	chr7:102254600-102257000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr7:102254600-102257000	Weak transcription	Fetal Muscle Leg	muscle
28	chr7:102254600-102257000	Weak transcription	Fetal Thymus	thymus
29	chr7:102254600-102257000	Weak transcription	Ovary	ovary
30	chr7:102254600-102257000	Weak transcription	Right Atrium	heart
31	chr7:102254600-102257400	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr7:102254600-102257600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr7:102254600-102257800	Weak transcription	Primary B cells from peripheral blood	blood
34	chr7:102257000-102257200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr7:102257000-102257200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr7:102257000-102257200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr7:102257000-102257200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr7:102257000-102257200	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr7:102257000-102257200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
40	chr7:102257000-102257200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
41	chr7:102257000-102257200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr7:102257000-102257200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr7:102257000-102257200	Active TSS	Adipose Nuclei	Adipose
44	chr7:102257000-102257200	Active TSS	Brain Inferior Temporal Lobe	brain
45	chr7:102257000-102257200	Enhancers	Colonic Mucosa	Colon
46	chr7:102257000-102257200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
47	chr7:102257000-102257200	Enhancers	Fetal Muscle Leg	muscle
48	chr7:102257000-102257200	Enhancers	Placenta	Placenta
49	chr7:102257000-102257200	Flanking Active TSS	K562	blood
50	chr7:102257000-102257400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived

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