Variant report

Variant	nsv5964
Chromosome Location	chr7:137599451-137616300
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:238)
CpG islands
(count:122)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:238 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:137601995-137602665	GM12878	blood:	n/a	n/a
2	ATF2	chr7:137601266-137602854	GM12878	blood:	n/a	n/a
3	BACH1	chr7:137606365-137606469	K562	blood:	n/a	n/a
4	BATF	chr7:137601358-137601644	GM12878	blood:	n/a	n/a
5	BATF	chr7:137608260-137608569	GM12878	blood:	n/a	chr7:137608434-137608444 chr7:137608433-137608444
6	BCLAF1	chr7:137601092-137602774	GM12878	blood:	n/a	n/a
7	BHLHE40	chr7:137605030-137605045	K562	blood:	n/a	n/a
8	BRCA1	chr7:137604811-137604965	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr7:137600197-137600330	K562	blood:	n/a	n/a
10	CEBPB	chr7:137608103-137608547	IMR90	lung:	n/a	chr7:137608501-137608514
11	CEBPB	chr7:137606852-137606936	K562	blood:	n/a	n/a
12	CEBPB	chr7:137615357-137615813	IMR90	lung:	n/a	n/a
13	CEBPB	chr7:137600214-137600298	A549	lung:	n/a	n/a
14	CREB1	chr7:137607930-137608627	GM12878	blood:	n/a	n/a
15	CREB1	chr7:137608030-137608562	GM12878	blood:	n/a	n/a
16	CTCF	chr7:137614060-137614210	MCF-7	breast:	n/a	n/a
17	CTCF	chr7:137614091-137614266	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr7:137602600-137602750	GM06990	blood:	n/a	n/a
19	CTCF	chr7:137614120-137614270	HepG2	liver:	n/a	n/a
20	CTCF	chr7:137614169-137614228	HepG2	liver:	n/a	n/a
21	CTCF	chr7:137614160-137614310	HMEC	breast:	n/a	n/a
22	CTCF	chr7:137614100-137614250	HCPEpiC	choroid plexus:	n/a	n/a
23	CTCF	chr7:137614120-137614270	HVMF	connective:	n/a	n/a
24	CTCF	chr7:137614040-137614190	AG09309	skin:	n/a	n/a
25	CTCF	chr7:137614135-137614210	MCF-7	breast:	n/a	n/a
26	CTCF	chr7:137614122-137614236	MCF-7	breast:	n/a	n/a
27	CTCF	chr7:137614100-137614250	BJ	skin:	n/a	n/a
28	CTCF	chr7:137614120-137614270	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr7:137614060-137614210	HMF	breast:	n/a	n/a
30	CTCF	chr7:137614128-137614197	MCF-7	breast:	n/a	n/a
31	CTCF	chr7:137614118-137614232	K562	blood:	n/a	n/a
32	CTCF	chr7:137614120-137614270	HA-sp	spinal cord:	n/a	n/a
33	CTCF	chr7:137614059-137614256	HepG2	liver:	n/a	n/a
34	CTCF	chr7:137614148-137614183	NHEK	skin:	n/a	n/a
35	CTCF	chr7:137614120-137614270	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr7:137614060-137614210	AG10803	skin:	n/a	n/a
37	CTCF	chr7:137608400-137608550	GM12873	blood:	n/a	n/a
38	CTCF	chr7:137614031-137614250	K562	blood:	n/a	n/a
39	CTCF	chr7:137602753-137602861	GM12878	blood:	n/a	n/a
40	CTCF	chr7:137614140-137614290	A549	lung:	n/a	n/a
41	CTCF	chr7:137614037-137614331	K562	blood:	n/a	n/a
42	CTCF	chr7:137614100-137614250	AG10803	skin:	n/a	n/a
43	CTCF	chr7:137614120-137614270	AG04449	skin:	n/a	n/a
44	CTCF	chr7:137614100-137614250	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr7:137614139-137614203	MCF-7	breast:	n/a	n/a
46	E2F4	chr7:137615472-137615722	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr7:137607686-137607864	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr7:137608083-137608318	MCF10A-Er-Src	breast:	n/a	n/a
49	ELF1	chr7:137601175-137601636	GM12878	blood:	n/a	n/a
50	ELF1	chr7:137601131-137601597	GM12878	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:137609343-137609393	Hela-S3	cervix:	n/a
2	chr7:137605253-137605303	AoSMC	blood vessel:	n/a
3	chr7:137609343-137609393	AoSMC	blood vessel:	n/a
4	chr7:137605253-137605303	SK-N-SH	brain:	n/a
5	chr7:137609343-137609393	NHDF-neo	bronchial:	n/a
6	chr7:137605253-137605303	HCT-116	colon:	n/a
7	chr7:137605253-137605303	NT2-D1	testis:	n/a
8	chr7:137605253-137605303	GM12878	blood:	n/a
9	chr7:137605253-137605303	HIPEpiC	eye:	n/a
10	chr7:137609343-137609393	HCF	heart:	n/a
11	chr7:137609343-137609393	LNCaP	prostate:	n/a
12	chr7:137609343-137609393	NHBE	bronchial:	n/a
13	chr7:137609343-137609393	PrEC	prostate:	n/a
14	chr7:137609343-137609393	PANC-1	pancreas:	n/a
15	chr7:137609343-137609393	IMR90	lung:	fetal
16	chr7:137609343-137609393	GM12891	blood:	n/a
17	chr7:137605253-137605303	CMK	blood:	n/a
18	chr7:137605253-137605303	SAEC	small airway:	n/a
19	chr7:137609343-137609393	NB4	blood:	n/a
20	chr7:137605253-137605303	LNCaP	prostate:	n/a
21	chr7:137605253-137605303	HAEpiC	amniotic membrane:	n/a
22	chr7:137605253-137605303	HEK293	kidney:	embryo
23	chr7:137609343-137609393	NT2-D1	testis:	n/a
24	chr7:137605253-137605303	ovcar-3	ovarian:	n/a
25	chr7:137609343-137609393	HUVEC	blood vessel:	n/a
26	chr7:137609343-137609393	GM12878	blood:	n/a
27	chr7:137609343-137609393	Hepatocyte	liver:	n/a
28	chr7:137605253-137605303	MCF10A-Er-Src	breast:	n/a
29	chr7:137605253-137605303	BE2_C	brain:	n/a
30	chr7:137605253-137605303	HEEpiC	esophagus:	n/a
31	chr7:137609343-137609393	ProgFib	skin:	n/a
32	chr7:137605253-137605303	SK-N-MC	brain:	n/a
33	chr7:137605253-137605303	AG04450	lung:	fetal
34	chr7:137609343-137609393	HNPCEpiC	eye:	n/a
35	chr7:137605253-137605303	SK-N-SH_RA	brain:	n/a
36	chr7:137605253-137605303	NB4	blood:	n/a
37	chr7:137605253-137605303	GM06990	blood:	n/a
38	chr7:137605253-137605303	Jurkat	blood:	n/a
39	chr7:137605253-137605303	H1-hESC	embryonic stem cell:	embryo
40	chr7:137605253-137605303	HRPEpiC	eye:	n/a
41	chr7:137605253-137605303	Caco-2	colon:	n/a
42	chr7:137605253-137605303	ECC-1	luminal epithelium:	n/a
43	chr7:137609343-137609393	A549	lung:	n/a
44	chr7:137605253-137605303	NHDF-neo	bronchial:	n/a
45	chr7:137605253-137605303	HCM	heart:	n/a
46	chr7:137609343-137609393	MCF-7	breast:	n/a
47	chr7:137605253-137605303	SKMC	muscle:	n/a
48	chr7:137609343-137609393	HCM	heart:	n/a
49	chr7:137605253-137605303	HPAEpiC	pulmonary alveolar:	n/a
50	chr7:137609343-137609393	HCPEpiC	choroid plexus:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:137602936..137605750-chr7:137611145..137614286,3	K562	blood:
2	chr17:57917876..57919842-chr7:137604891..137607469,2	MCF-7	breast:
3	chr7:137594343..137597893-chr7:137600589..137603730,5	K562	blood:
4	chr7:137611854..137613484-chr7:137685563..137687785,2	K562	blood:
5	chr7:137602934..137605506-chr7:137607486..137609542,3	K562	blood:
6	chr7:137601809..137604434-chr7:137608042..137610252,2	K562	blood:
7	chr7:137600305..137602461-chr7:137615591..137618449,2	MCF-7	breast:
8	chr7:137609204..137611818-chr7:137677756..137679539,2	K562	blood:
9	chr7:137600305..137602461-chr7:137615591..137618449,2	MCF-7	breast:
10	chr7:137601426..137603845-chr7:137616116..137618626,2	K562	blood:
11	chr7:137611909..137614588-chr7:137616790..137618864,2	K562	blood:
12	chr7:137601426..137603845-chr7:137616116..137618626,2	K562	blood:
13	chr7:137601809..137604434-chr7:137608042..137610252,2	K562	blood:
14	chr7:137600116..137601742-chr7:137606169..137608041,2	K562	blood:
15	chr7:137598519..137601964-chr7:137608334..137611661,3	K562	blood:
16	chr7:137602934..137605506-chr7:137607486..137609542,3	K562	blood:
17	chr7:137609953..137612415-chr7:137663430..137666120,2	K562	blood:
18	chr7:137607730..137610117-chr7:137638239..137640378,2	MCF-7	breast:
19	chr7:137594343..137597312-chr7:137601337..137603443,2	K562	blood:
20	chr7:137600116..137601742-chr7:137606169..137608041,2	K562	blood:
21	chr7:137606279..137609116-chr7:137617759..137619750,2	K562	blood:
22	chr7:137600116..137602105-chr7:137606169..137608041,3	K562	blood:
23	chr7:137615597..137618364-chr7:137618491..137620760,2	K562	blood:
24	chr7:137600116..137602105-chr7:137606169..137608041,3	K562	blood:
25	chr7:137598519..137601964-chr7:137608334..137611661,3	K562	blood:
26	chr7:137608254..137611336-chr7:137611630..137614398,3	K562	blood:

No data

Variant related genes	Relation type
CREB3L2	TF binding region
CREB3L2	CpG island
ENSG00000122787	chromatin interactions
ENSG00000182158	chromatin interactions
ENSG00000199004	chromatin interactions

Extended variants
information (count: 676 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:676 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553177002	chr7:137599592-137599593	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs6467725	chr7:137599609-137599610	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs567142435	chr7:137599613-137599614	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs201867636	chr7:137599641-137599642	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs557715794	chr7:137599645-137599646	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs536051350	chr7:137599677-137599678	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs569448476	chr7:137599709-137599710	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs538361361	chr7:137599726-137599727	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs7792041	chr7:137599748-137599749	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs577819611	chr7:137599751-137599752	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs534183424	chr7:137599762-137599763	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs554487069	chr7:137599798-137599799	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs186212101	chr7:137599910-137599911	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs543034456	chr7:137599922-137599923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191063348	chr7:137599932-137599933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs59616289	chr7:137599978-137599979	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs545523804	chr7:137600030-137600031	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs116100238	chr7:137600031-137600032	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs527523940	chr7:137600034-137600035	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs34491918	chr7:137600092-137600093	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs377765207	chr7:137600125-137600126	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575183197	chr7:137600158-137600159	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs113928415	chr7:137600208-137600209	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182359465	chr7:137600209-137600210	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs369120342	chr7:137600234-137600235	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554388589	chr7:137600311-137600312	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186576667	chr7:137600379-137600380	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs544379475	chr7:137600380-137600381	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs7777310	chr7:137600385-137600386	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs529644092	chr7:137600386-137600387	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs77681427	chr7:137600424-137600425	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs569331947	chr7:137600441-137600442	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs538300051	chr7:137600502-137600503	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs574537005	chr7:137600511-137600512	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs373878627	chr7:137600567-137600568	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs200625961	chr7:137600568-137600569	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs139796301	chr7:137600583-137600584	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs537687504	chr7:137600597-137600598	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs201981192	chr7:137600626-137600627	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs376931481	chr7:137600644-137600645	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147928164	chr7:137600658-137600659	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201136941	chr7:137600663-137600664	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs200109348	chr7:137600681-137600682	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145713623	chr7:137600682-137600683	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs273957	chr7:137600690-137600691	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs143530987	chr7:137600739-137600740	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs115655218	chr7:137600758-137600759	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs576514426	chr7:137600785-137600786	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs73456329	chr7:137600810-137600811	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs111998854	chr7:137600823-137600824	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Neuroticism	17667963	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute myeloid leukemia	17237825	CNVD
Esophageal cancer	21851588	CNVD
Bladder cancer	21909424	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell acute lymphoblastic leukemia	16673021	CNVD
Cancer	21183584	CNVD
Intracranial ependymoma	16609018	CNVD
Non-small cell lung cancer	21829676	CNVD
Developmental delay	19490664	CNVD
Pancreatitis	20877625	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Cancer	17440070	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:137584200-137601000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr7:137584200-137612000	Weak transcription	Fetal Brain Male	brain
3	chr7:137584400-137601600	Strong transcription	Fetal Intestine Large	intestine
4	chr7:137584600-137604800	Weak transcription	Right Atrium	heart
5	chr7:137585000-137604800	Weak transcription	Psoas Muscle	Psoas
6	chr7:137585000-137605800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
7	chr7:137585200-137601000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr7:137585200-137606200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr7:137587600-137600200	Strong transcription	Left Ventricle	heart
10	chr7:137588800-137599800	Weak transcription	NHEK	skin
11	chr7:137588800-137600800	Strong transcription	Adipose Nuclei	Adipose
12	chr7:137588800-137600800	Strong transcription	Rectal Mucosa Donor 31	rectum
13	chr7:137588800-137601400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr7:137588800-137601600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr7:137588800-137603400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr7:137588800-137603400	Strong transcription	Fetal Intestine Small	intestine
17	chr7:137588800-137606200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr7:137588800-137615400	Weak transcription	Stomach Mucosa	stomach
19	chr7:137588800-137618400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr7:137588800-137620200	Weak transcription	Dnd41	blood
21	chr7:137589000-137600800	Strong transcription	Stomach Smooth Muscle	stomach
22	chr7:137589000-137601000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr7:137589000-137601600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr7:137589000-137601600	Strong transcription	Liver	Liver
25	chr7:137589000-137602800	Strong transcription	HepG2	liver
26	chr7:137589000-137606200	Strong transcription	Monocytes-CD14+_RO01746	blood
27	chr7:137589400-137600800	Strong transcription	Primary T helper cells fromperipheralblood	blood
28	chr7:137589400-137600800	Strong transcription	Duodenum Mucosa	Duodenum
29	chr7:137589400-137600800	Strong transcription	Rectal Mucosa Donor 29	rectum
30	chr7:137589400-137603600	Strong transcription	NHLF	lung
31	chr7:137589400-137603800	Strong transcription	Sigmoid Colon	Sigmoid Colon
32	chr7:137589600-137600000	Strong transcription	Lung	lung
33	chr7:137589600-137600200	Strong transcription	H1 Cell Line	embryonic stem cell
34	chr7:137589600-137601400	Strong transcription	Primary neutrophils fromperipheralblood	blood
35	chr7:137589600-137601600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr7:137589600-137613600	Strong transcription	Primary monocytes fromperipheralblood	blood
37	chr7:137589800-137601000	Strong transcription	Primary B cells from peripheral blood	blood
38	chr7:137589800-137601000	Strong transcription	Primary T cells fromperipheralblood	blood
39	chr7:137589800-137601800	Strong transcription	Primary hematopoietic stem cells	blood
40	chr7:137590000-137603000	Strong transcription	Fetal Stomach	stomach
41	chr7:137590000-137603400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr7:137590200-137600000	Strong transcription	Cortex derived primary cultured neurospheres	brain
43	chr7:137590200-137600400	Strong transcription	GM12878-XiMat	blood
44	chr7:137590200-137600800	Strong transcription	Primary T cells from cord blood	blood
45	chr7:137590200-137600800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr7:137590200-137600800	Strong transcription	Duodenum Smooth Muscle	Duodenum
47	chr7:137590200-137601000	Strong transcription	Fetal Lung	lung
48	chr7:137590200-137601000	Strong transcription	HSMM	muscle
49	chr7:137590400-137600200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr7:137590400-137600200	Strong transcription	Fetal Muscle Leg	muscle

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