Variant report

Variant	nsv981570
Chromosome Location	chr7:108213540-108214810
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:9)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:9 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CUX1	chr7:108213832-108213840	GM12878	blood:	n/a	n/a
2	CUX1	chr7:108214249-108214462	K562	blood:	n/a	n/a
3	E2F4	chr7:108214313-108214680	MCF10A-Er-Src	breast:	n/a	n/a
4	POLR2A	chr7:108213593-108217498	HepG2	liver:	n/a	n/a
5	POLR2A	chr7:108214148-108214541	HepG2	liver:	n/a	n/a
6	POLR2A	chr7:108214541-108214550	MCF10A-Er-Src	breast:	n/a	n/a
7	POLR2A	chr7:108199426-108221976	K562	blood:	n/a	n/a
8	TBL1XR1	chr7:108214128-108214900	K562	blood:	n/a	n/a
9	ZC3H11A	chr7:108214549-108214669	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:108213750-108213800	LNCaP	prostate:	n/a
2	chr7:108213750-108213800	PANC-1	pancreas:	n/a
3	chr7:108213750-108213800	HEEpiC	esophagus:	n/a
4	chr7:108213750-108213800	AG09309	skin:	n/a
5	chr7:108213750-108213800	AoSMC	blood vessel:	n/a
6	chr7:108213750-108213800	BE2_C	brain:	n/a
7	chr7:108213750-108213800	K562	blood:	n/a
8	chr7:108213750-108213800	GM12878	blood:	n/a
9	chr7:108213750-108213800	AG04450	lung:	fetal
10	chr7:108213750-108213800	SK-N-MC	brain:	n/a
11	chr7:108213750-108213800	HRCEpiC	kidney:	n/a
12	chr7:108213750-108213800	AG09319	gingival:	n/a
13	chr7:108213750-108213800	Jurkat	blood:	n/a
14	chr7:108213750-108213800	BJ	skin:	n/a
15	chr7:108213750-108213800	HL-60	blood:	n/a
16	chr7:108213750-108213800	HEK293	kidney:	embryo
17	chr7:108213750-108213800	MCF10A-Er-Src	breast:	n/a
18	chr7:108213750-108213800	HIPEpiC	eye:	n/a
19	chr7:108213750-108213800	IMR90	lung:	fetal
20	chr7:108213750-108213800	ProgFib	skin:	n/a
21	chr7:108213750-108213800	HUVEC	blood vessel:	n/a
22	chr7:108213750-108213800	CMK	blood:	n/a
23	chr7:108213750-108213800	HCT-116	colon:	n/a
24	chr7:108213750-108213800	GM12891	blood:	n/a
25	chr7:108213750-108213800	SKMC	muscle:	n/a
26	chr7:108213750-108213800	HNPCEpiC	eye:	n/a
27	chr7:108213750-108213800	SK-N-SH_RA	brain:	n/a
28	chr7:108213750-108213800	RPTEC	kidney:	n/a
29	chr7:108213750-108213800	NHBE	bronchial:	n/a
30	chr7:108213750-108213800	HPAEpiC	pulmonary alveolar:	n/a
31	chr7:108213750-108213800	NH-A	brain:	n/a
32	chr7:108213750-108213800	SK-N-SH	brain:	n/a
33	chr7:108213750-108213800	HCM	heart:	n/a
34	chr7:108213750-108213800	GM06990	blood:	n/a
35	chr7:108213750-108213800	GM19239	blood:	n/a
36	chr7:108213750-108213800	GM12892	blood:	n/a
37	chr7:108213750-108213800	NB4	blood:	n/a
38	chr7:108213750-108213800	HMEC	breast:	n/a
39	chr7:108213750-108213800	HCPEpiC	choroid plexus:	n/a
40	chr7:108213750-108213800	MCF-7	breast:	n/a
41	chr7:108213750-108213800	HAEpiC	amniotic membrane:	n/a
42	chr7:108213750-108213800	PFSK-1	brain:	n/a
43	chr7:108213750-108213800	SAEC	small airway:	n/a
44	chr7:108213750-108213800	A549	lung:	n/a
45	chr7:108213750-108213800	AG10803	skin:	n/a
46	chr7:108213750-108213800	Caco-2	colon:	n/a
47	chr7:108213750-108213800	T-47D	breast:	n/a
48	chr7:108213750-108213800	HepG2	liver:	n/a
49	chr7:108213750-108213800	AG04449	skin:	fetal
50	chr7:108213750-108213800	Hela-S3	cervix:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:108159403..108171484-chr7:108200740..108214365,45	K562	blood:
2	chr7:108163136..108166047-chr7:108214620..108217426,3	K562	blood:
3	chr7:107786172..107787859-chr7:108212708..108215561,2	MCF-7	breast:
4	chr7:108209600..108213665-chr7:112090307..112092525,3	K562	blood:
5	chr7:108162967..108170259-chr7:108208242..108216228,25	MCF-7	breast:
6	chr7:108213141..108217464-chr7:108225107..108230596,8	K562	blood:
7	chr7:108143422..108146244-chr7:108213317..108215644,2	K562	blood:
8	chr7:108163122..108173185-chr7:108207236..108216619,40	K562	blood:

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	DNAJB9	hsa-miR-32-5p	chr7:108214638-108214662
2	DNAJB9	hsa-miR-505-3p	chr7:108213814-108213834
3	DNAJB9	hsa-miR-32-5p	chr7:108214656-108214677
4	DNAJB9	hsa-miR-32-5p	chr7:108214670-108214677

Variant related genes	Relation type
THAP5	TF binding region
PNPLA8	TF binding region
THAP5	CpG island
PNPLA8	CpG island
ENSG00000135241	chromatin interactions
ENSG00000006652	chromatin interactions

Extended variants
information (count: 45 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:45 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376971670	chr7:108213545-108213546	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs201325742	chr7:108213556-108213557	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs371348305	chr7:108213564-108213565	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs150713685	chr7:108213585-108213586	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs267601234	chr7:108213604-108213605	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs139507326	chr7:108213647-108213648	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs147747165	chr7:108213690-108213691	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs199929387	chr7:108213723-108213724	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs142486892	chr7:108213734-108213735	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs149830505	chr7:108213739-108213740	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs182601197	chr7:108213761-108213762	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs550166034	chr7:108213763-108213764	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs201481756	chr7:108213790-108213791	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs200296116	chr7:108213792-108213793	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs539029657	chr7:108213806-108213807	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs187252724	chr7:108213811-108213812	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs371758437	chr7:108213825-108213826	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region miRNA target site	4 gene(s)	Overlapped CNVs	n/a
18	rs375296782	chr7:108213833-108213834	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region miRNA target site	4 gene(s)	Overlapped CNVs	n/a
19	rs368994075	chr7:108213841-108213842	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs192021096	chr7:108213906-108213907	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs3763457	chr7:108213926-108213927	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs11408141	chr7:108213939-108213940	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs73428112	chr7:108214100-108214101	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs377765156	chr7:108214102-108214103	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs3763456	chr7:108214119-108214120	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs3763455	chr7:108214131-108214132	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs147964164	chr7:108214152-108214153	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs577345709	chr7:108214195-108214196	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs546198697	chr7:108214216-108214217	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs546419128	chr7:108214222-108214223	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs183438831	chr7:108214248-108214249	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs188843857	chr7:108214283-108214284	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs542069377	chr7:108214290-108214291	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs562265068	chr7:108214301-108214302	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs531133352	chr7:108214304-108214305	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs550830726	chr7:108214353-108214354	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs566651601	chr7:108214368-108214369	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs570785153	chr7:108214436-108214437	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs4727712	chr7:108214445-108214446	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs559356585	chr7:108214502-108214503	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs538965165	chr7:108214519-108214520	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs193080310	chr7:108214683-108214684	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs546176562	chr7:108214712-108214713	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs566451900	chr7:108214713-108214714	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs141839050	chr7:108214753-108214754	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	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
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
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Autism	19401682	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD

Chromatin state (count:182 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:108211200-108214200	Weak transcription	Small Intestine	intestine
2	chr7:108211200-108219400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:108211200-108219600	Weak transcription	Lung	lung
4	chr7:108211400-108215400	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr7:108211400-108216600	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr7:108211400-108217400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr7:108211400-108219400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr7:108211400-108219600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr7:108211400-108219600	Weak transcription	Colonic Mucosa	Colon
10	chr7:108211400-108219600	Weak transcription	Esophagus	oesophagus
11	chr7:108211400-108219600	Weak transcription	Ovary	ovary
12	chr7:108211400-108219800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr7:108211600-108213600	Weak transcription	HSMMtube	muscle
14	chr7:108211600-108214400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr7:108211600-108215800	Weak transcription	Thymus	Thymus
16	chr7:108211600-108219200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr7:108211600-108219200	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr7:108211600-108219400	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr7:108211600-108219400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr7:108211600-108220000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr7:108211800-108214600	Weak transcription	Stomach Mucosa	stomach
22	chr7:108211800-108218400	Weak transcription	NHLF	lung
23	chr7:108211800-108219800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr7:108212000-108214800	Genic enhancers	Primary T helper memory cells from peripheral blood 1	blood
25	chr7:108212000-108219400	Weak transcription	Brain Germinal Matrix	brain
26	chr7:108212000-108219600	Weak transcription	Fetal Stomach	stomach
27	chr7:108212000-108222600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr7:108212200-108213600	Enhancers	Fetal Brain Male	brain
29	chr7:108212200-108214800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr7:108212200-108219400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr7:108212200-108219600	Weak transcription	Brain Hippocampus Middle	brain
32	chr7:108212200-108219800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr7:108212400-108213600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr7:108212400-108213600	Weak transcription	Left Ventricle	heart
35	chr7:108212400-108213800	Enhancers	Fetal Heart	heart
36	chr7:108212400-108214400	Weak transcription	Brain Cingulate Gyrus	brain
37	chr7:108212400-108214600	Weak transcription	Brain Angular Gyrus	brain
38	chr7:108212400-108215400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr7:108212400-108215600	Weak transcription	Pancreas	Pancrea
40	chr7:108212400-108215800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
41	chr7:108212400-108215800	Weak transcription	Adipose Nuclei	Adipose
42	chr7:108212400-108216400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr7:108212400-108216400	Strong transcription	HUES64 Cell Line	embryonic stem cell
44	chr7:108212400-108216600	Strong transcription	HUES48 Cell Line	embryonic stem cell
45	chr7:108212400-108217200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr7:108212400-108219200	Weak transcription	Fetal Brain Female	brain
47	chr7:108212400-108219400	Weak transcription	Aorta	Aorta
48	chr7:108212400-108219400	Weak transcription	Brain Anterior Caudate	brain
49	chr7:108212400-108219400	Weak transcription	Fetal Intestine Small	intestine
50	chr7:108212400-108219400	Weak transcription	Gastric	stomach

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