Variant report

Variant	nsv1007141
Chromosome Location	chr3:158415840-158433128
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:252)
CpG islands
(count:123)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:252 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr3:158430240-158430593	GM12878	blood:	n/a	chr3:158430440-158430449
2	BATF	chr3:158429600-158430020	GM12878	blood:	n/a	chr3:158429780-158429790 chr3:158429779-158429790
3	BHLHE40	chr3:158430554-158431343	K562	blood:	n/a	n/a
4	CTCF	chr3:158420220-158420370	HCPEpiC	choroid plexus:	n/a	n/a
5	CTCF	chr3:158420220-158420370	HRE	kidney:	n/a	n/a
6	CTCF	chr3:158420148-158420429	IMR90	lung:	n/a	n/a
7	CTCF	chr3:158420160-158420310	AG10803	skin:	n/a	n/a
8	CTCF	chr3:158420160-158420310	HMF	breast:	n/a	n/a
9	CTCF	chr3:158427620-158427770	HBMEC	blood vessel:	n/a	n/a
10	CTCF	chr3:158431900-158432050	HCPEpiC	choroid plexus:	n/a	n/a
11	CTCF	chr3:158427460-158427610	AG09319	gingival:	n/a	n/a
12	CTCF	chr3:158420180-158420330	MCF-7	breast:	n/a	n/a
13	CTCF	chr3:158427620-158427770	HCPEpiC	choroid plexus:	n/a	n/a
14	CTCF	chr3:158420280-158420430	AoAF	blood vessel:	n/a	n/a
15	CTCF	chr3:158420140-158420290	NHDF-neo	bronchial:	n/a	n/a
16	CTCF	chr3:158420040-158420190	A549	lung:	n/a	n/a
17	CTCF	chr3:158420160-158420310	HPF	lung:	n/a	n/a
18	CTCF	chr3:158420200-158420350	HMF	breast:	n/a	n/a
19	CTCF	chr3:158427320-158427470	AG09319	gingival:	n/a	n/a
20	CTCF	chr3:158420260-158420410	BJ	skin:	n/a	n/a
21	CTCF	chr3:158420140-158420290	HVMF	connective:	n/a	n/a
22	CTCF	chr3:158420260-158420410	NHLF	lung:	n/a	n/a
23	CTCF	chr3:158420320-158420470	AG04450	lung:	n/a	n/a
24	CTCF	chr3:158420100-158420250	AG04450	lung:	n/a	n/a
25	CTCF	chr3:158420100-158420250	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr3:158420240-158420390	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr3:158427440-158427590	AG10803	skin:	n/a	n/a
28	CTCF	chr3:158420180-158420330	HCFaa	heart:	n/a	n/a
29	CTCF	chr3:158420220-158420370	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr3:158420160-158420310	AG04450	lung:	n/a	n/a
31	CTCF	chr3:158427340-158427490	NHDF-neo	bronchial:	n/a	n/a
32	CTCF	chr3:158420200-158420350	AG04449	skin:	n/a	n/a
33	CTCF	chr3:158423418-158423463	Spleen_OC	spleen:	n/a	n/a
34	CTCF	chr3:158420160-158420310	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr3:158427680-158427830	AG04449	skin:	n/a	n/a
36	CTCF	chr3:158427420-158427570	NHLF	lung:	n/a	n/a
37	CTCF	chr3:158420160-158420310	HFF	foreskin:	n/a	n/a
38	CTCF	chr3:158420100-158420370	HVMF	connective:	n/a	n/a
39	E2F4	chr3:158419551-158419703	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr3:158429792-158429894	MCF10A-Er-Src	breast:	n/a	n/a
41	EP300	chr3:158418157-158418871	SK-N-SH	brain:	n/a	n/a
42	EP300	chr3:158427307-158427889	SK-N-SH_RA	brain:	n/a	n/a
43	EP300	chr3:158418251-158418759	SK-N-SH_RA	brain:	n/a	n/a
44	EP300	chr3:158427215-158427888	SK-N-SH_RA	brain:	n/a	n/a
45	EP300	chr3:158429798-158429845	K562	blood:	n/a	n/a
46	EP300	chr3:158427576-158427678	K562	blood:	n/a	n/a
47	EP300	chr3:158419024-158419034	GM12878	blood:	n/a	n/a
48	EP300	chr3:158420838-158421196	SK-N-SH_RA	brain:	n/a	n/a
49	EP300	chr3:158427166-158427973	SK-N-SH	brain:	n/a	chr3:158427919-158427933
50	EP300	chr3:158418260-158418830	SK-N-SH_RA	brain:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:158427635-158427685	HCM	heart:	n/a
2	chr3:158427635-158427685	HCM	heart:	n/a
3	chr3:158430962-158431012	SK-N-SH	brain:	n/a
4	chr3:158427635-158427685	NT2-D1	testis:	n/a
5	chr3:158427635-158427685	SK-N-SH	brain:	n/a
6	chr3:158430962-158431012	Jurkat	blood:	n/a
7	chr3:158430962-158431012	HCM	heart:	n/a
8	chr3:158430962-158431012	HCT-116	colon:	n/a
9	chr3:158427635-158427685	U87	brain:	n/a
10	chr3:158430962-158431012	CMK	blood:	n/a
11	chr3:158427635-158427685	GM12891	blood:	n/a
12	chr3:158430962-158431012	HMEC	breast:	n/a
13	chr3:158430962-158431012	Hepatocyte	liver:	n/a
14	chr3:158427635-158427685	HRE	kidney:	n/a
15	chr3:158430962-158431012	HCF	heart:	n/a
16	chr3:158430962-158431012	RPTEC	kidney:	n/a
17	chr3:158427635-158427685	PANC-1	pancreas:	n/a
18	chr3:158430962-158431012	HL-60	blood:	n/a
19	chr3:158430962-158431012	HRPEpiC	eye:	n/a
20	chr3:158430962-158431012	NT2-D1	testis:	n/a
21	chr3:158430962-158431012	HPAEpiC	pulmonary alveolar:	n/a
22	chr3:158427635-158427685	CMK	blood:	n/a
23	chr3:158427635-158427685	ECC-1	luminal epithelium:	n/a
24	chr3:158427635-158427685	A549	lung:	n/a
25	chr3:158430962-158431012	AG09319	gingival:	n/a
26	chr3:158427635-158427685	SK-N-SH_RA	brain:	n/a
27	chr3:158430962-158431012	ovcar-3	ovarian:	n/a
28	chr3:158427635-158427685	HAEpiC	amniotic membrane:	n/a
29	chr3:158427635-158427685	NB4	blood:	n/a
30	chr3:158427635-158427685	NH-A	brain:	n/a
31	chr3:158427635-158427685	LNCaP	prostate:	n/a
32	chr3:158430962-158431012	HAEpiC	amniotic membrane:	n/a
33	chr3:158430962-158431012	HCPEpiC	choroid plexus:	n/a
34	chr3:158430962-158431012	AG04450	lung:	fetal
35	chr3:158430962-158431012	MCF10A-Er-Src	breast:	n/a
36	chr3:158427635-158427685	SK-N-MC	brain:	n/a
37	chr3:158427635-158427685	AG04450	lung:	fetal
38	chr3:158430962-158431012	BE2_C	brain:	n/a
39	chr3:158427635-158427685	Hepatocyte	liver:	n/a
40	chr3:158427635-158427685	HIPEpiC	eye:	n/a
41	chr3:158430962-158431012	AoSMC	blood vessel:	n/a
42	chr3:158430962-158431012	T-47D	breast:	n/a
43	chr3:158430962-158431012	SK-N-SH_RA	brain:	n/a
44	chr3:158430962-158431012	AG04449	skin:	fetal
45	chr3:158427635-158427685	H1-hESC	embryonic stem cell:	embryo
46	chr3:158427635-158427685	Jurkat	blood:	n/a
47	chr3:158430962-158431012	AG09309	skin:	n/a
48	chr3:158430962-158431012	HRE	kidney:	n/a
49	chr3:158430962-158431012	HEEpiC	esophagus:	n/a
50	chr3:158427635-158427685	NHBE	bronchial:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:158431830..158434181-chr3:158437291..158439276,2	MCF-7	breast:
2	chr3:158415231..158418143-chr3:158424169..158428339,3	MCF-7	breast:
3	chr3:158421107..158423161-chr3:158433354..158436179,2	K562	blood:
4	chr3:158361580..158364350-chr3:158421426..158423181,2	K562	blood:
5	chr3:158423211..158426282-chr3:158428433..158432187,3	K562	blood:
6	chr3:158430342..158432825-chr3:158434955..158438595,5	K562	blood:
7	chr3:158425598..158427216-chr3:158443542..158445810,2	K562	blood:
8	chr3:158422890..158425062-chr3:158426331..158429823,3	MCF-7	breast:
9	chr3:158429563..158432825-chr3:158433996..158437681,6	K562	blood:
10	chr3:158431692..158434686-chr3:158440756..158442982,2	K562	blood:
11	chr3:158423141..158424731-chr3:158426844..158428477,2	K562	blood:
12	chr3:158423211..158426282-chr3:158428433..158432187,3	K562	blood:
13	chr3:158388083..158390320-chr3:158417482..158420125,2	MCF-7	breast:
14	chr3:158422890..158425062-chr3:158426331..158429823,3	MCF-7	breast:
15	chr3:158429468..158431337-chr3:158439788..158442505,2	MCF-7	breast:
16	chr3:158389157..158390779-chr3:158425576..158427091,2	MCF-7	breast:
17	chr3:158415231..158418143-chr3:158424169..158428339,3	MCF-7	breast:
18	chr3:158419005..158421589-chr3:158422766..158427522,4	K562	blood:
19	chr3:158431752..158433309-chr3:158518750..158520621,2	K562	blood:
20	chr3:158415825..158417591-chr3:158438376..158440279,2	MCF-7	breast:

No data

Variant related genes	Relation type
RARRES1	TF binding region
ENSG00000272087	TF binding region
RARRES1	CpG island
ENSG00000272087	CpG island
ENSG00000118849	chromatin interactions
ENSG00000079257	chromatin interactions
ENSG00000168827	chromatin interactions
ENSG00000118855	chromatin interactions
ENSG00000272247	chromatin interactions

Extended variants
information (count: 628 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:628 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3867391	chr3:158415840-158415841	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs561958107	chr3:158415862-158415863	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542446579	chr3:158415883-158415884	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs6772483	chr3:158415999-158416000	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs190727704	chr3:158416044-158416045	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs115183553	chr3:158416060-158416061	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564138130	chr3:158416067-158416068	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs528060992	chr3:158416097-158416098	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs16847123	chr3:158416137-158416138	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs371153205	chr3:158416408-158416409	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs16829314	chr3:158416409-158416410	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs573919149	chr3:158416419-158416420	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs11448918	chr3:158416466-158416467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs201902690	chr3:158416477-158416478	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs78596381	chr3:158416478-158416479	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs73156490	chr3:158416484-158416485	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs141169208	chr3:158416490-158416491	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs150477270	chr3:158416493-158416494	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs181584968	chr3:158416511-158416512	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs534732375	chr3:158416539-158416540	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73156491	chr3:158416572-158416573	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs185753164	chr3:158416576-158416577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs7621897	chr3:158416646-158416647	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs557634518	chr3:158416700-158416701	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs575886510	chr3:158416745-158416746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs545918736	chr3:158416753-158416754	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564044100	chr3:158416759-158416760	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs138353174	chr3:158416763-158416764	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs73156492	chr3:158416799-158416800	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs561714213	chr3:158416837-158416838	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs141076686	chr3:158416851-158416852	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs57805621	chr3:158416870-158416871	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs73030851	chr3:158416952-158416953	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs568743460	chr3:158416958-158416959	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs532973547	chr3:158416959-158416960	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs551523790	chr3:158416969-158416970	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs2713731	chr3:158416973-158416974	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs149612984	chr3:158416974-158416975	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs553135912	chr3:158417001-158417002	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs147288972	chr3:158417045-158417046	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs190407752	chr3:158417110-158417111	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs13323588	chr3:158417174-158417175	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs375100963	chr3:158417193-158417194	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs370855437	chr3:158417223-158417224	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs377479542	chr3:158417230-158417231	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs369613039	chr3:158417231-158417232	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs397777001	chr3:158417233-158417234	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs76002071	chr3:158417234-158417235	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs558288658	chr3:158417254-158417255	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs572890979	chr3:158417265-158417266	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Breast cancer	21364760	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:692 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:158390400-158416800	Weak transcription	Aorta	Aorta
2	chr3:158390400-158428600	Weak transcription	Brain Cingulate Gyrus	brain
3	chr3:158390600-158427400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr3:158390800-158416800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr3:158390800-158425400	Weak transcription	Fetal Brain Female	brain
6	chr3:158390800-158427000	Weak transcription	Brain Angular Gyrus	brain
7	chr3:158390800-158427400	Weak transcription	Esophagus	oesophagus
8	chr3:158390800-158427400	Weak transcription	Lung	lung
9	chr3:158390800-158429400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr3:158390800-158430200	Weak transcription	Brain Hippocampus Middle	brain
11	chr3:158390800-158430400	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr3:158390800-158430800	Weak transcription	Right Ventricle	heart
13	chr3:158390800-158430800	Weak transcription	Stomach Mucosa	stomach
14	chr3:158390800-158432800	Weak transcription	Spleen	Spleen
15	chr3:158390800-158444200	Weak transcription	Gastric	stomach
16	chr3:158390800-158445400	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr3:158391000-158418600	Weak transcription	Fetal Brain Male	brain
18	chr3:158391000-158421000	Weak transcription	Fetal Heart	heart
19	chr3:158391000-158427200	Weak transcription	NHEK	skin
20	chr3:158391000-158427400	Weak transcription	Pancreas	Pancrea
21	chr3:158391000-158429200	Weak transcription	Colon Smooth Muscle	Colon
22	chr3:158391000-158430600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr3:158391000-158438800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr3:158395800-158420800	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr3:158395800-158423000	Weak transcription	Fetal Stomach	stomach
26	chr3:158396200-158418400	Weak transcription	Brain Germinal Matrix	brain
27	chr3:158397000-158429200	Weak transcription	Ovary	ovary
28	chr3:158397000-158443400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr3:158397000-158448000	Weak transcription	Thymus	Thymus
30	chr3:158397800-158425200	Weak transcription	HSMMtube	muscle
31	chr3:158399600-158445400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr3:158400600-158429000	Weak transcription	Brain Substantia Nigra	brain
33	chr3:158403600-158438600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
34	chr3:158403800-158420800	Weak transcription	HMEC	breast
35	chr3:158408000-158417800	Strong transcription	Fetal Intestine Large	intestine
36	chr3:158408400-158430200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
37	chr3:158408400-158443000	Weak transcription	HepG2	liver
38	chr3:158408600-158419400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr3:158408800-158422400	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr3:158409000-158429800	Weak transcription	Small Intestine	intestine
41	chr3:158409200-158421200	Weak transcription	Psoas Muscle	Psoas
42	chr3:158409200-158427400	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr3:158409400-158425400	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr3:158409400-158425600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr3:158409400-158426200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr3:158409400-158426800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
47	chr3:158409400-158427200	Weak transcription	Brain Anterior Caudate	brain
48	chr3:158409600-158417600	Weak transcription	NHDF-Ad	bronchial
49	chr3:158409800-158439000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
50	chr3:158410000-158424200	Weak transcription	Rectal Mucosa Donor 31	rectum

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