Variant report

Variant	nsv888908
Chromosome Location	chr7:102245449-102339168
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2954)
CpG islands
(count:977)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2954 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr7:102312022-102312401	A549	lung:	n/a	chr7:102312144-102312152
2	ATF3	chr7:102312099-102312242	K562	blood:	n/a	chr7:102312144-102312152
3	BATF	chr7:102285771-102286300	GM12878	blood:	n/a	chr7:102286082-102286093
4	BATF	chr7:102251367-102251812	GM12878	blood:	n/a	n/a
5	BATF	chr7:102329824-102330101	GM12878	blood:	n/a	n/a
6	BATF	chr7:102312293-102312492	GM12878	blood:	n/a	n/a
7	BATF	chr7:102284603-102285287	GM12878	blood:	n/a	n/a
8	BATF	chr7:102266316-102266513	GM12878	blood:	n/a	n/a
9	BATF	chr7:102306478-102306740	GM12878	blood:	n/a	n/a
10	BATF	chr7:102278828-102279089	GM12878	blood:	n/a	n/a
11	BATF	chr7:102252871-102253062	GM12878	blood:	n/a	n/a
12	BATF	chr7:102254763-102255038	GM12878	blood:	n/a	n/a
13	BATF	chr7:102310540-102311004	GM12878	blood:	n/a	n/a
14	BATF	chr7:102285752-102286469	GM12878	blood:	n/a	chr7:102286082-102286093
15	BATF	chr7:102313180-102313439	GM12878	blood:	n/a	n/a
16	BATF	chr7:102254253-102254722	GM12878	blood:	n/a	n/a
17	BATF	chr7:102256202-102256653	GM12878	blood:	n/a	n/a
18	BATF	chr7:102291963-102292217	GM12878	blood:	n/a	n/a
19	BATF	chr7:102286810-102287040	GM12878	blood:	n/a	n/a
20	BATF	chr7:102278880-102279149	GM12878	blood:	n/a	n/a
21	BATF	chr7:102311459-102312701	GM12878	blood:	n/a	n/a
22	BATF	chr7:102247244-102247556	GM12878	blood:	n/a	n/a
23	BATF	chr7:102305017-102305524	GM12878	blood:	n/a	n/a
24	BATF	chr7:102257362-102257620	GM12878	blood:	n/a	n/a
25	BATF	chr7:102254118-102255225	GM12878	blood:	n/a	n/a
26	BATF	chr7:102293584-102293766	GM12878	blood:	n/a	n/a
27	BATF	chr7:102330287-102330744	GM12878	blood:	n/a	n/a
28	BATF	chr7:102284765-102285178	GM12878	blood:	n/a	n/a
29	BATF	chr7:102310144-102310402	GM12878	blood:	n/a	n/a
30	BATF	chr7:102313151-102313476	GM12878	blood:	n/a	n/a
31	BCL11A	chr7:102313169-102313449	GM12878	blood:	n/a	n/a
32	BCL11A	chr7:102255171-102255360	GM12878	blood:	n/a	chr7:102255318-102255331
33	BCL11A	chr7:102291947-102292248	GM12878	blood:	n/a	n/a
34	BCL11A	chr7:102284155-102284333	GM12878	blood:	n/a	n/a
35	BCL11A	chr7:102256150-102256705	GM12878	blood:	n/a	chr7:102256299-102256308
36	BCL11A	chr7:102311440-102312266	GM12878	blood:	n/a	n/a
37	BCL11A	chr7:102266323-102266491	GM12878	blood:	n/a	n/a
38	BCL11A	chr7:102283861-102284058	GM12878	blood:	n/a	n/a
39	BCL11A	chr7:102291566-102291715	GM12878	blood:	n/a	n/a
40	BCL11A	chr7:102254129-102255412	GM12878	blood:	n/a	chr7:102255318-102255331 chr7:102254203-102254212
41	BCL11A	chr7:102284599-102285236	GM12878	blood:	n/a	n/a
42	BCL11A	chr7:102310787-102310962	GM12878	blood:	n/a	n/a
43	BCL11A	chr7:102301177-102301426	GM12878	blood:	n/a	n/a
44	BCL11A	chr7:102296701-102296848	GM12878	blood:	n/a	n/a
45	BCL11A	chr7:102312275-102312544	GM12878	blood:	n/a	chr7:102312277-102312290
46	BCL11A	chr7:102304517-102304823	GM12878	blood:	n/a	n/a
47	BCL11A	chr7:102251198-102251922	GM12878	blood:	n/a	chr7:102251388-102251397
48	BCL11A	chr7:102285737-102286323	GM12878	blood:	n/a	n/a
49	BCL11A	chr7:102310539-102310728	GM12878	blood:	n/a	n/a
50	BCL11A	chr7:102284553-102285170	GM12878	blood:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102327236-102327286	HEEpiC	esophagus:	n/a
2	chr7:102327236-102327286	HEEpiC	esophagus:	n/a
3	chr7:102332458-102332508	HCM	heart:	n/a
4	chr7:102329146-102329196	HPAEpiC	pulmonary alveolar:	n/a
5	chr7:102259241-102259291	HL-60	blood:	n/a
6	chr7:102313412-102313462	GM12891	blood:	n/a
7	chr7:102312315-102312365	HIPEpiC	eye:	n/a
8	chr7:102308061-102308111	RPTEC	kidney:	n/a
9	chr7:102332458-102332508	SK-N-SH_RA	brain:	n/a
10	chr7:102312200-102312250	PFSK-1	brain:	n/a
11	chr7:102312318-102312368	GM19239	blood:	n/a
12	chr7:102308061-102308111	HRCEpiC	kidney:	n/a
13	chr7:102312315-102312365	Hela-S3	cervix:	n/a
14	chr7:102308061-102308111	HEK293	kidney:	embryo
15	chr7:102313389-102313439	U87	brain:	n/a
16	chr7:102312308-102312358	AG10803	skin:	n/a
17	chr7:102332458-102332508	Hepatocyte	liver:	n/a
18	chr7:102308061-102308111	SK-N-SH	brain:	n/a
19	chr7:102330635-102330685	ProgFib	skin:	n/a
20	chr7:102312315-102312365	IMR90	lung:	fetal
21	chr7:102327236-102327286	GM19239	blood:	n/a
22	chr7:102327236-102327286	SK-N-SH	brain:	n/a
23	chr7:102312331-102312381	HCPEpiC	choroid plexus:	n/a
24	chr7:102312318-102312368	MCF-7	breast:	n/a
25	chr7:102327236-102327286	AG04449	skin:	fetal
26	chr7:102312308-102312358	SK-N-MC	brain:	n/a
27	chr7:102313389-102313439	LNCaP	prostate:	n/a
28	chr7:102246378-102246428	RPTEC	kidney:	n/a
29	chr7:102313389-102313439	HMEC	breast:	n/a
30	chr7:102313412-102313462	NT2-D1	testis:	n/a
31	chr7:102312331-102312381	H1-hESC	embryonic stem cell:	embryo
32	chr7:102259241-102259291	MCF-7	breast:	n/a
33	chr7:102329146-102329196	HRE	kidney:	n/a
34	chr7:102312331-102312381	AG09309	skin:	n/a
35	chr7:102311965-102312015	HEK293	kidney:	embryo
36	chr7:102329146-102329196	NH-A	brain:	n/a
37	chr7:102332458-102332508	LNCaP	prostate:	n/a
38	chr7:102312315-102312365	K562	blood:	n/a
39	chr7:102312308-102312358	HEK293	kidney:	embryo
40	chr7:102330635-102330685	Jurkat	blood:	n/a
41	chr7:102312308-102312358	HCT-116	colon:	n/a
42	chr7:102327236-102327286	HCM	heart:	n/a
43	chr7:102246378-102246428	NHBE	bronchial:	n/a
44	chr7:102332458-102332508	HMEC	breast:	n/a
45	chr7:102308061-102308111	AG09319	gingival:	n/a
46	chr7:102313412-102313462	IMR90	lung:	fetal
47	chr7:102332458-102332508	HRE	kidney:	n/a
48	chr7:102246378-102246428	BE2_C	brain:	n/a
49	chr7:102312318-102312368	HRE	kidney:	n/a
50	chr7:102308061-102308111	IMR90	lung:	fetal

No data

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

Extended variants
information (count: 1138 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1138 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527509828	chr7:102245581-102245582	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs113743857	chr7:102245817-102245818	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs377036068	chr7:102245884-102245885	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs371426553	chr7:102245893-102245894	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs370599958	chr7:102246002-102246003	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs199959861	chr7:102246110-102246111	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs549145539	chr7:102246123-102246124	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs200892777	chr7:102246147-102246148	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs568475711	chr7:102246154-102246155	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs535915195	chr7:102246184-102246185	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs200495391	chr7:102246209-102246210	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs149631316	chr7:102246225-102246226	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs557088079	chr7:102246271-102246272	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs376229544	chr7:102246277-102246278	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs11547189	chr7:102246311-102246312	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs569276008	chr7:102246353-102246354	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs539444438	chr7:102246365-102246366	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs139960113	chr7:102246366-102246367	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs369222056	chr7:102246385-102246386	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs142342278	chr7:102246394-102246395	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs540444029	chr7:102246400-102246401	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs372956201	chr7:102246402-102246403	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs151024405	chr7:102246410-102246411	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs140941587	chr7:102246427-102246428	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
25	rs200418348	chr7:102246447-102246448	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs375655267	chr7:102246476-102246477	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs144574884	chr7:102246500-102246501	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs573660638	chr7:102246546-102246547	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs544253095	chr7:102246551-102246552	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs562430721	chr7:102246596-102246597	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs369242220	chr7:102246649-102246650	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs112315952	chr7:102246687-102246688	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs555519087	chr7:102246843-102246844	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs372619645	chr7:102246961-102246962	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs533003924	chr7:102247113-102247114	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs530052250	chr7:102247121-102247122	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs544996794	chr7:102247250-102247251	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs147906944	chr7:102247659-102247660	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs560473901	chr7:102247863-102247864	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs527547662	chr7:102247876-102247877	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs548926999	chr7:102248415-102248416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567407589	chr7:102248452-102248453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531397403	chr7:102248479-102248480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551101577	chr7:102248489-102248490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568990074	chr7:102248495-102248496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs372805684	chr7:102248723-102248724	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs371759940	chr7:102248724-102248725	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs375186482	chr7:102250136-102250137	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs113207428	chr7:102250208-102250209	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs539483159	chr7:102250314-102250315	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

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

Chromatin state (count:474 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102236200-102252400	Weak transcription	Fetal Muscle Leg	muscle
2	chr7:102242400-102246000	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr7:102242600-102252400	Weak transcription	Ovary	ovary
4	chr7:102244200-102252400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr7:102244200-102252400	Weak transcription	Lung	lung
6	chr7:102244200-102252400	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr7:102244400-102246000	Weak transcription	Hela-S3	cervix
8	chr7:102244800-102252400	Weak transcription	Fetal Stomach	stomach
9	chr7:102245200-102252400	Weak transcription	Fetal Brain Female	brain
10	chr7:102246000-102246200	Enhancers	Hela-S3	cervix
11	chr7:102246000-102246400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr7:102246000-102246800	Enhancers	Skeletal Muscle Female	skeletal muscle
13	chr7:102246000-102246800	Enhancers	K562	blood
14	chr7:102246000-102252400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr7:102246400-102246800	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr7:102246400-102252200	Weak transcription	Stomach Smooth Muscle	stomach
17	chr7:102246400-102252400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr7:102246800-102251000	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr7:102246800-102252400	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr7:102246800-102252400	Weak transcription	K562	blood
21	chr7:102251000-102251200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr7:102251000-102251200	Enhancers	Primary B cells from peripheral blood	blood
23	chr7:102251000-102251200	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr7:102251000-102251200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr7:102251000-102251200	Enhancers	Skeletal Muscle Female	skeletal muscle
26	chr7:102251000-102251200	Enhancers	A549	lung
27	chr7:102251000-102251200	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr7:102251200-102252200	Weak transcription	A549	lung
29	chr7:102251200-102252200	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr7:102251200-102252400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr7:102251200-102252400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr7:102251200-102252400	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr7:102251400-102252400	Weak transcription	Primary B cells from peripheral blood	blood
34	chr7:102251400-102252400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr7:102252200-102252400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr7:102252200-102252400	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr7:102252200-102252400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr7:102252200-102252400	Enhancers	Adipose Nuclei	Adipose
39	chr7:102252200-102252400	Enhancers	Brain Anterior Caudate	brain
40	chr7:102252200-102252400	Enhancers	Rectal Smooth Muscle	rectum
41	chr7:102252200-102252400	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr7:102252200-102252400	Enhancers	Stomach Smooth Muscle	stomach
43	chr7:102252200-102252400	Enhancers	Dnd41	blood
44	chr7:102252200-102252400	Enhancers	GM12878-XiMat	blood
45	chr7:102252200-102252400	Active TSS	Monocytes-CD14+_RO01746	blood
46	chr7:102252200-102252800	Enhancers	Primary B cells from cord blood	blood
47	chr7:102252200-102252800	Enhancers	Fetal Brain Male	brain
48	chr7:102252200-102252800	Enhancers	A549	lung
49	chr7:102252400-102252600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr7:102252400-102252600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived

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