Variant report

Variant	nsv888861
Chromosome Location	chr7:102151310-102334106
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:6040)
CpG islands
(count:1282)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:6040 , 50 per page) page: 1 2 3 4 5 6 7 ... 121

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	chr7:102312099-102312242	K562	blood:	n/a	chr7:102312144-102312152
4	ATF3	chr7:102213014-102213188	K562	blood:	n/a	n/a
5	ATF3	chr7:102312022-102312401	A549	lung:	n/a	chr7:102312144-102312152
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	chr7:102167226-102167423	GM12878	blood:	n/a	n/a
9	BATF	chr7:102310540-102311004	GM12878	blood:	n/a	n/a
10	BATF	chr7:102329824-102330101	GM12878	blood:	n/a	n/a
11	BATF	chr7:102192870-102193124	GM12878	blood:	n/a	n/a
12	BATF	chr7:102285771-102286300	GM12878	blood:	n/a	chr7:102286082-102286093
13	BATF	chr7:102192070-102192285	GM12878	blood:	n/a	n/a
14	BATF	chr7:102187719-102187949	GM12878	blood:	n/a	n/a
15	BATF	chr7:102278828-102279089	GM12878	blood:	n/a	n/a
16	BATF	chr7:102284765-102285178	GM12878	blood:	n/a	n/a
17	BATF	chr7:102186680-102187209	GM12878	blood:	n/a	chr7:102186991-102187002
18	BATF	chr7:102306478-102306740	GM12878	blood:	n/a	n/a
19	BATF	chr7:102284603-102285287	GM12878	blood:	n/a	n/a
20	BATF	chr7:102155274-102155743	GM12878	blood:	n/a	n/a
21	BATF	chr7:102313180-102313439	GM12878	blood:	n/a	n/a
22	BATF	chr7:102185674-102186087	GM12878	blood:	n/a	n/a
23	BATF	chr7:102186661-102187378	GM12878	blood:	n/a	chr7:102186991-102187002
24	BATF	chr7:102257362-102257620	GM12878	blood:	n/a	n/a
25	BATF	chr7:102285752-102286469	GM12878	blood:	n/a	chr7:102286082-102286093
26	BATF	chr7:102286810-102287040	GM12878	blood:	n/a	n/a
27	BATF	chr7:102212695-102213163	GM12878	blood:	n/a	n/a
28	BATF	chr7:102312293-102312492	GM12878	blood:	n/a	n/a
29	BATF	chr7:102278880-102279149	GM12878	blood:	n/a	n/a
30	BATF	chr7:102233914-102234227	GM12878	blood:	n/a	n/a
31	BATF	chr7:102256202-102256653	GM12878	blood:	n/a	n/a
32	BATF	chr7:102305017-102305524	GM12878	blood:	n/a	n/a
33	BATF	chr7:102179720-102179981	GM12878	blood:	n/a	n/a
34	BATF	chr7:102313151-102313476	GM12878	blood:	n/a	n/a
35	BATF	chr7:102214079-102214404	GM12878	blood:	n/a	n/a
36	BATF	chr7:102252871-102253062	GM12878	blood:	n/a	n/a
37	BATF	chr7:102254253-102254722	GM12878	blood:	n/a	n/a
38	BATF	chr7:102330287-102330744	GM12878	blood:	n/a	n/a
39	BATF	chr7:102234392-102234834	GM12878	blood:	n/a	n/a
40	BATF	chr7:102152206-102152651	GM12878	blood:	n/a	n/a
41	BATF	chr7:102155784-102156059	GM12878	blood:	n/a	n/a
42	BATF	chr7:102153892-102154083	GM12878	blood:	n/a	n/a
43	BATF	chr7:102311459-102312701	GM12878	blood:	n/a	n/a
44	BATF	chr7:102207398-102207660	GM12878	blood:	n/a	n/a
45	BATF	chr7:102291963-102292217	GM12878	blood:	n/a	n/a
46	BATF	chr7:102254118-102255225	GM12878	blood:	n/a	n/a
47	BATF	chr7:102254763-102255038	GM12878	blood:	n/a	n/a
48	BATF	chr7:102266316-102266513	GM12878	blood:	n/a	n/a
49	BATF	chr7:102251367-102251812	GM12878	blood:	n/a	n/a
50	BATF	chr7:102211460-102211924	GM12878	blood:	n/a	n/a

(count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102311965-102312015	NB4	blood:	n/a
2	chr7:102311965-102312015	NB4	blood:	n/a
3	chr7:102312331-102312381	HCT-116	colon:	n/a
4	chr7:102196182-102196232	RPTEC	kidney:	n/a
5	chr7:102212892-102212942	HL-60	blood:	n/a
6	chr7:102279588-102279638	RPTEC	kidney:	n/a
7	chr7:102155527-102155577	HAEpiC	amniotic membrane:	n/a
8	chr7:102312308-102312358	HCM	heart:	n/a
9	chr7:102312308-102312358	AG09309	skin:	n/a
10	chr7:102158209-102158259	HIPEpiC	eye:	n/a
11	chr7:102332458-102332508	NT2-D1	testis:	n/a
12	chr7:102312308-102312358	MCF-7	breast:	n/a
13	chr7:102332458-102332508	HMEC	breast:	n/a
14	chr7:102246378-102246428	HCM	heart:	n/a
15	chr7:102246378-102246428	AG10803	skin:	n/a
16	chr7:102196182-102196232	AG10803	skin:	n/a
17	chr7:102279588-102279638	GM12892	blood:	n/a
18	chr7:102155527-102155577	AG10803	skin:	n/a
19	chr7:102158209-102158259	HCT-116	colon:	n/a
20	chr7:102312315-102312365	A549	lung:	n/a
21	chr7:102329146-102329196	A549	lung:	n/a
22	chr7:102161506-102161556	SK-N-MC	brain:	n/a
23	chr7:102279588-102279638	AoSMC	blood vessel:	n/a
24	chr7:102279588-102279638	HepG2	liver:	n/a
25	chr7:102259241-102259291	GM12878	blood:	n/a
26	chr7:102246378-102246428	HL-60	blood:	n/a
27	chr7:102313412-102313462	PrEC	prostate:	n/a
28	chr7:102196182-102196232	HCPEpiC	choroid plexus:	n/a
29	chr7:102329146-102329196	NHBE	bronchial:	n/a
30	chr7:102330635-102330685	HNPCEpiC	eye:	n/a
31	chr7:102312315-102312365	MCF-7	breast:	n/a
32	chr7:102312315-102312365	AG09309	skin:	n/a
33	chr7:102308061-102308111	SK-N-MC	brain:	n/a
34	chr7:102246378-102246428	ECC-1	luminal epithelium:	n/a
35	chr7:102327236-102327286	SK-N-MC	brain:	n/a
36	chr7:102158209-102158259	SK-N-SH	brain:	n/a
37	chr7:102332458-102332508	SK-N-SH_RA	brain:	n/a
38	chr7:102196182-102196232	PrEC	prostate:	n/a
39	chr7:102279588-102279638	SKMC	muscle:	n/a
40	chr7:102246378-102246428	NH-A	brain:	n/a
41	chr7:102327236-102327286	LNCaP	prostate:	n/a
42	chr7:102313412-102313462	AG04450	lung:	fetal
43	chr7:102196182-102196232	T-47D	breast:	n/a
44	chr7:102196182-102196232	CMK	blood:	n/a
45	chr7:102313389-102313439	NB4	blood:	n/a
46	chr7:102308061-102308111	HCM	heart:	n/a
47	chr7:102312315-102312365	HIPEpiC	eye:	n/a
48	chr7:102332458-102332508	MCF10A-Er-Src	breast:	n/a
49	chr7:102246378-102246428	HRCEpiC	kidney:	n/a
50	chr7:102327236-102327286	PFSK-1	brain:	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
RASA4B	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
ENSG00000238392	TF binding region
ENSG00000270249	CpG island
RASA4B	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
ENSG00000238392	CpG island

Extended variants
information (count: 1858 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1858 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77603563	chr7:102151310-102151311	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs571879004	chr7:102151535-102151536	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs62484826	chr7:102151821-102151822	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs374353921	chr7:102151926-102151927	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs372670057	chr7:102152804-102152805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs377723117	chr7:102152837-102152838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs371084346	chr7:102152943-102152944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs374229027	chr7:102153021-102153022	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs377276733	chr7:102153098-102153099	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs181077647	chr7:102153138-102153139	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs186003609	chr7:102153151-102153152	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs536260420	chr7:102153286-102153287	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs539293833	chr7:102153299-102153300	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs71559476	chr7:102153330-102153331	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs71559477	chr7:102153337-102153338	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs554077287	chr7:102153407-102153408	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
17	rs62484827	chr7:102153445-102153446	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
18	rs374395070	chr7:102153576-102153577	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
19	rs369476607	chr7:102153636-102153637	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs543236880	chr7:102153641-102153642	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs551379688	chr7:102153650-102153651	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs367575078	chr7:102153814-102153815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554751992	chr7:102153839-102153840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576185027	chr7:102153847-102153848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs144153426	chr7:102154200-102154201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs62484829	chr7:102154558-102154559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372295591	chr7:102154666-102154667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs147516383	chr7:102154667-102154668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543478775	chr7:102155168-102155169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs564864535	chr7:102155204-102155205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs140160974	chr7:102155221-102155222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs150251382	chr7:102155235-102155236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs532325174	chr7:102155247-102155248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs71559480	chr7:102155527-102155528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs149016620	chr7:102157347-102157348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs367759102	chr7:102157722-102157723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541271336	chr7:102158021-102158022	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs559294331	chr7:102158051-102158052	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs529878817	chr7:102158194-102158195	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs375392175	chr7:102158806-102158807	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs372229746	chr7:102158815-102158816	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs567445769	chr7:102158818-102158819	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs373391720	chr7:102158819-102158820	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs200127378	chr7:102158820-102158821	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs549921587	chr7:102158824-102158825	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs571572070	chr7:102158829-102158830	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs538975720	chr7:102158833-102158834	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs113733198	chr7:102158839-102158840	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs71205769	chr7:102158858-102158859	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs373174667	chr7:102158859-102158860	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Schizophrenia	20967226	CNVD
Pancreatic cancer	17952125	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:957 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102119400-102153000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr7:102119400-102153200	Weak transcription	Ovary	ovary
3	chr7:102143600-102153000	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr7:102146600-102153000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr7:102146800-102153000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr7:102146800-102153000	Weak transcription	Osteobl	bone
7	chr7:102147000-102158600	Weak transcription	Hela-S3	cervix
8	chr7:102147400-102153000	Weak transcription	Brain Angular Gyrus	brain
9	chr7:102147400-102153200	Weak transcription	Fetal Muscle Trunk	muscle
10	chr7:102148200-102153000	Weak transcription	A549	lung
11	chr7:102148200-102153000	Weak transcription	K562	blood
12	chr7:102148200-102153000	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr7:102148200-102153200	Weak transcription	Fetal Thymus	thymus
14	chr7:102149400-102153200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr7:102150600-102152800	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr7:102152800-102153000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
17	chr7:102152800-102153000	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr7:102152800-102153000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
19	chr7:102152800-102153000	Enhancers	Primary T helper cells fromperipheralblood	blood
20	chr7:102152800-102153000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
21	chr7:102152800-102153000	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr7:102152800-102153000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr7:102152800-102153000	Enhancers	Brain Anterior Caudate	brain
24	chr7:102152800-102153000	Enhancers	Brain Substantia Nigra	brain
25	chr7:102152800-102153000	Enhancers	Dnd41	blood
26	chr7:102153000-102153200	Active TSS	H9 Cell Line	embryonic stem cell
27	chr7:102153000-102153200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr7:102153000-102153200	Active TSS	Breast Myoepithelial Primary Cells	Breast
29	chr7:102153000-102153200	Active TSS	Primary monocytes fromperipheralblood	blood
30	chr7:102153000-102153200	Enhancers	Primary T cells fromperipheralblood	blood
31	chr7:102153000-102153200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr7:102153000-102153200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr7:102153000-102153200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr7:102153000-102153200	Enhancers	Brain Germinal Matrix	brain
35	chr7:102153000-102153200	Active TSS	Brain Hippocampus Middle	brain
36	chr7:102153000-102153200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
37	chr7:102153000-102153200	Active TSS	Colon Smooth Muscle	Colon
38	chr7:102153000-102153200	Active TSS	Duodenum Smooth Muscle	Duodenum
39	chr7:102153000-102153200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
40	chr7:102153000-102153200	Active TSS	Fetal Muscle Leg	muscle
41	chr7:102153000-102153200	Active TSS	Left Ventricle	heart
42	chr7:102153000-102153200	Active TSS	Right Atrium	heart
43	chr7:102153000-102153200	Enhancers	NH-A	brain
44	chr7:102153000-102153200	Enhancers	NHDF-Ad	bronchial
45	chr7:102153000-102153400	Active TSS	H1 Cell Line	embryonic stem cell
46	chr7:102153000-102153400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr7:102153000-102153400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr7:102153000-102153400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr7:102153000-102153400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr7:102153000-102153400	Active TSS	HUES6 Cell Line	embryonic stem cell

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