Variant report

Variant	nsv888867
Chromosome Location	chr7:102183897-102339168
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4880)
CpG islands
(count:1100)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:4880 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

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	ATF3	chr7:102213014-102213141	GM12878	blood:	n/a	n/a
3	ATF3	chr7:102312099-102312242	K562	blood:	n/a	chr7:102312144-102312152
4	ATF3	chr7:102312022-102312401	A549	lung:	n/a	chr7:102312144-102312152
5	ATF3	chr7:102213014-102213188	K562	blood:	n/a	n/a
6	BACH1	chr7:102213021-102213172	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr7:102254763-102255038	GM12878	blood:	n/a	n/a
8	BATF	chr7:102234392-102234834	GM12878	blood:	n/a	n/a
9	BATF	chr7:102192070-102192285	GM12878	blood:	n/a	n/a
10	BATF	chr7:102286810-102287040	GM12878	blood:	n/a	n/a
11	BATF	chr7:102251367-102251812	GM12878	blood:	n/a	n/a
12	BATF	chr7:102214079-102214404	GM12878	blood:	n/a	n/a
13	BATF	chr7:102330287-102330744	GM12878	blood:	n/a	n/a
14	BATF	chr7:102285752-102286469	GM12878	blood:	n/a	chr7:102286082-102286093
15	BATF	chr7:102278828-102279089	GM12878	blood:	n/a	n/a
16	BATF	chr7:102254118-102255225	GM12878	blood:	n/a	n/a
17	BATF	chr7:102306478-102306740	GM12878	blood:	n/a	n/a
18	BATF	chr7:102212379-102213628	GM12878	blood:	n/a	n/a
19	BATF	chr7:102312293-102312492	GM12878	blood:	n/a	n/a
20	BATF	chr7:102252871-102253062	GM12878	blood:	n/a	n/a
21	BATF	chr7:102329824-102330101	GM12878	blood:	n/a	n/a
22	BATF	chr7:102233914-102234227	GM12878	blood:	n/a	n/a
23	BATF	chr7:102185510-102186196	GM12878	blood:	n/a	n/a
24	BATF	chr7:102310144-102310402	GM12878	blood:	n/a	n/a
25	BATF	chr7:102214085-102214343	GM12878	blood:	n/a	n/a
26	BATF	chr7:102257362-102257620	GM12878	blood:	n/a	n/a
27	BATF	chr7:102305017-102305524	GM12878	blood:	n/a	n/a
28	BATF	chr7:102212695-102213163	GM12878	blood:	n/a	n/a
29	BATF	chr7:102247244-102247556	GM12878	blood:	n/a	n/a
30	BATF	chr7:102192870-102193124	GM12878	blood:	n/a	n/a
31	BATF	chr7:102186661-102187378	GM12878	blood:	n/a	chr7:102186991-102187002
32	BATF	chr7:102205933-102206440	GM12878	blood:	n/a	n/a
33	BATF	chr7:102293584-102293766	GM12878	blood:	n/a	n/a
34	BATF	chr7:102285771-102286300	GM12878	blood:	n/a	chr7:102286082-102286093
35	BATF	chr7:102284603-102285287	GM12878	blood:	n/a	n/a
36	BATF	chr7:102310540-102311004	GM12878	blood:	n/a	n/a
37	BATF	chr7:102207398-102207660	GM12878	blood:	n/a	n/a
38	BATF	chr7:102311459-102312701	GM12878	blood:	n/a	n/a
39	BATF	chr7:102313151-102313476	GM12878	blood:	n/a	n/a
40	BATF	chr7:102185674-102186087	GM12878	blood:	n/a	n/a
41	BATF	chr7:102256202-102256653	GM12878	blood:	n/a	n/a
42	BATF	chr7:102254253-102254722	GM12878	blood:	n/a	n/a
43	BATF	chr7:102284765-102285178	GM12878	blood:	n/a	n/a
44	BATF	chr7:102186680-102187209	GM12878	blood:	n/a	chr7:102186991-102187002
45	BATF	chr7:102211064-102211322	GM12878	blood:	n/a	n/a
46	BATF	chr7:102313180-102313439	GM12878	blood:	n/a	n/a
47	BATF	chr7:102291963-102292217	GM12878	blood:	n/a	n/a
48	BATF	chr7:102187719-102187949	GM12878	blood:	n/a	n/a
49	BATF	chr7:102266316-102266513	GM12878	blood:	n/a	n/a
50	BATF	chr7:102211460-102211924	GM12878	blood:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102332458-102332508	Jurkat	blood:	n/a
2	chr7:102312318-102312368	HepG2	liver:	n/a
3	chr7:102332458-102332508	Jurkat	blood:	n/a
4	chr7:102312318-102312368	HepG2	liver:	n/a
5	chr7:102313412-102313462	HCF	heart:	n/a
6	chr7:102246378-102246428	PFSK-1	brain:	n/a
7	chr7:102196182-102196232	ECC-1	luminal epithelium:	n/a
8	chr7:102246378-102246428	HIPEpiC	eye:	n/a
9	chr7:102196182-102196232	MCF-7	breast:	n/a
10	chr7:102279588-102279638	AG04449	skin:	fetal
11	chr7:102311965-102312015	AG04449	skin:	fetal
12	chr7:102308061-102308111	Jurkat	blood:	n/a
13	chr7:102312318-102312368	NT2-D1	testis:	n/a
14	chr7:102311965-102312015	NHDF-neo	bronchial:	n/a
15	chr7:102329146-102329196	BJ	skin:	n/a
16	chr7:102212892-102212942	GM12892	blood:	n/a
17	chr7:102329146-102329196	HCPEpiC	choroid plexus:	n/a
18	chr7:102311965-102312015	SK-N-MC	brain:	n/a
19	chr7:102329146-102329196	GM12891	blood:	n/a
20	chr7:102313389-102313439	Jurkat	blood:	n/a
21	chr7:102327236-102327286	GM12878	blood:	n/a
22	chr7:102332458-102332508	HCF	heart:	n/a
23	chr7:102259241-102259291	PFSK-1	brain:	n/a
24	chr7:102312315-102312365	HL-60	blood:	n/a
25	chr7:102308061-102308111	GM12891	blood:	n/a
26	chr7:102279588-102279638	Caco-2	colon:	n/a
27	chr7:102312318-102312368	SAEC	small airway:	n/a
28	chr7:102312318-102312368	K562	blood:	n/a
29	chr7:102196182-102196232	SKMC	muscle:	n/a
30	chr7:102330635-102330685	H1-hESC	embryonic stem cell:	embryo
31	chr7:102212892-102212942	T-47D	breast:	n/a
32	chr7:102312331-102312381	ECC-1	luminal epithelium:	n/a
33	chr7:102330635-102330685	ProgFib	skin:	n/a
34	chr7:102329146-102329196	LNCaP	prostate:	n/a
35	chr7:102308061-102308111	HRPEpiC	eye:	n/a
36	chr7:102327236-102327286	NH-A	brain:	n/a
37	chr7:102313412-102313462	NHDF-neo	bronchial:	n/a
38	chr7:102308061-102308111	AG09319	gingival:	n/a
39	chr7:102308061-102308111	SAEC	small airway:	n/a
40	chr7:102312318-102312368	GM06990	blood:	n/a
41	chr7:102246378-102246428	NHBE	bronchial:	n/a
42	chr7:102259241-102259291	RPTEC	kidney:	n/a
43	chr7:102279588-102279638	GM12891	blood:	n/a
44	chr7:102312331-102312381	SAEC	small airway:	n/a
45	chr7:102313412-102313462	PANC-1	pancreas:	n/a
46	chr7:102279588-102279638	NHDF-neo	bronchial:	n/a
47	chr7:102279588-102279638	SKMC	muscle:	n/a
48	chr7:102313389-102313439	GM06990	blood:	n/a
49	chr7:102313389-102313439	HepG2	liver:	n/a
50	chr7:102311965-102312015	GM06990	blood:	n/a

No data

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

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

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

Extended variants
information (count: 1630 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1630 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1105028	chr7:102183897-102183898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs1105027	chr7:102183902-102183903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs62482965	chr7:102184233-102184234	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs372876807	chr7:102184315-102184316	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs377180423	chr7:102184316-102184317	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs200966579	chr7:102184321-102184322	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs141001107	chr7:102184323-102184324	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs549217868	chr7:102184396-102184397	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs369412088	chr7:102184410-102184411	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs567420368	chr7:102184448-102184449	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs372659936	chr7:102184476-102184477	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs376916146	chr7:102184546-102184547	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs371271156	chr7:102184570-102184571	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs145311467	chr7:102184576-102184577	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs201458204	chr7:102184608-102184609	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs199630921	chr7:102184612-102184613	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs113797247	chr7:102184636-102184637	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs201613244	chr7:102184654-102184655	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs150259374	chr7:102184716-102184717	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs535960397	chr7:102184718-102184719	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs557222837	chr7:102184754-102184755	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs28730948	chr7:102184763-102184764	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs200759290	chr7:102184779-102184780	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs375088743	chr7:102184810-102184811	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs201884094	chr7:102184819-102184820	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs371982862	chr7:102185298-102185299	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs2428444	chr7:102185487-102185488	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs75408048	chr7:102185490-102185491	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs2428443	chr7:102185515-102185516	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs369969067	chr7:102185620-102185621	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs533226848	chr7:102185715-102185716	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs369133817	chr7:102185940-102185941	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs575674931	chr7:102185957-102185958	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs539486496	chr7:102186986-102186987	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
35	rs373744070	chr7:102187013-102187014	Weak transcription Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
36	rs558100603	chr7:102187036-102187037	Weak transcription Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
37	rs367544924	chr7:102187120-102187121	Weak transcription Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
38	rs372929897	chr7:102187143-102187144	Weak transcription Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
39	rs373430671	chr7:102188112-102188113	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
40	rs375522798	chr7:102188233-102188234	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
41	rs542845443	chr7:102188279-102188280	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
42	rs372802384	chr7:102188304-102188305	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
43	rs375568509	chr7:102188318-102188319	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
44	rs573222928	chr7:102188333-102188334	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
45	rs377052463	chr7:102188348-102188349	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
46	rs369783436	chr7:102188399-102188400	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
47	rs200876660	chr7:102188432-102188433	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
48	rs372036060	chr7:102188595-102188596	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
49	rs540478994	chr7:102188627-102188628	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
50	rs376357528	chr7:102188634-102188635	Weak transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	21364760	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
abnormal development	18461090	CNVD

Chromatin state (count:690 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102165600-102188200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:102168600-102212600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr7:102172400-102188200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr7:102173600-102212600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr7:102173800-102186800	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr7:102174400-102188600	Weak transcription	Lung	lung
7	chr7:102174800-102212600	Weak transcription	Fetal Stomach	stomach
8	chr7:102184000-102186600	Weak transcription	Primary monocytes fromperipheralblood	blood
9	chr7:102185800-102186200	Enhancers	GM12878-XiMat	blood
10	chr7:102187000-102187200	Enhancers	Placenta Amnion	Placenta Amnion
11	chr7:102187000-102187400	Enhancers	Primary B cells from peripheral blood	blood
12	chr7:102200600-102212600	Weak transcription	Fetal Brain Female	brain
13	chr7:102203000-102212600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr7:102203600-102212600	Weak transcription	Lung	lung
15	chr7:102203800-102212600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr7:102203800-102212600	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr7:102203800-102212600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr7:102204600-102206200	Weak transcription	Primary neutrophils fromperipheralblood	blood
19	chr7:102204800-102212600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr7:102204800-102212600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr7:102204800-102212600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr7:102204800-102212600	Weak transcription	Spleen	Spleen
23	chr7:102205000-102212600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr7:102205000-102212600	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr7:102205000-102212600	Weak transcription	Brain Germinal Matrix	brain
26	chr7:102205000-102212600	Weak transcription	Left Ventricle	heart
27	chr7:102205600-102212600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr7:102205600-102212600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr7:102205600-102212600	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr7:102205600-102212600	Weak transcription	Placenta	Placenta
31	chr7:102206200-102207400	Strong transcription	Primary neutrophils fromperipheralblood	blood
32	chr7:102206200-102209800	Weak transcription	Fetal Muscle Leg	muscle
33	chr7:102206200-102212600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr7:102206200-102212600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr7:102206200-102212600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr7:102206200-102212600	Weak transcription	Adipose Nuclei	Adipose
37	chr7:102206200-102212600	Weak transcription	Brain Cingulate Gyrus	brain
38	chr7:102206200-102212600	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr7:102206200-102212600	Weak transcription	Fetal Thymus	thymus
40	chr7:102206200-102212600	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr7:102206200-102212600	Weak transcription	Thymus	Thymus
42	chr7:102206800-102212600	Weak transcription	Brain Angular Gyrus	brain
43	chr7:102206800-102212600	Weak transcription	Brain Hippocampus Middle	brain
44	chr7:102207200-102212600	Weak transcription	Primary B cells from cord blood	blood
45	chr7:102207400-102211000	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr7:102207400-102212600	Weak transcription	Primary neutrophils fromperipheralblood	blood
47	chr7:102207600-102209800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr7:102209200-102209400	Enhancers	NH-A	brain
49	chr7:102209400-102212600	Weak transcription	NH-A	brain
50	chr7:102209800-102210200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood

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