Variant report

Variant	esv13701
Chromosome Location	chr7:5607355-5611372
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:381)
CpG islands
(count:245)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:381 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:5610007-5610112	K562	blood:	n/a	n/a
2	BACH1	chr7:5609109-5609155	K562	blood:	n/a	n/a
3	BACH1	chr7:5609952-5609994	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:5609619-5609640	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr7:5609746-5610091	K562	blood:	n/a	chr7:5609990-5610006
6	BRCA1	chr7:5609094-5609142	GM12878	blood:	n/a	n/a
7	BRCA1	chr7:5609948-5610148	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr7:5609519-5610584	K562	blood:	n/a	n/a
9	CBX3	chr7:5607364-5607872	K562	blood:	n/a	n/a
10	CCNT2	chr7:5609650-5610150	K562	blood:	n/a	n/a
11	CEBPB	chr7:5609092-5609102	K562	blood:	n/a	n/a
12	CEBPB	chr7:5609000-5609288	HepG2	liver:	n/a	n/a
13	CEBPB	chr7:5608737-5609284	A549	lung:	n/a	n/a
14	CEBPB	chr7:5608931-5609227	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr7:5609709-5609980	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr7:5609934-5610339	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr7:5608923-5609276	Hela-S3	cervix:	n/a	n/a
18	CHD2	chr7:5609701-5610146	H1-hESC	embryonic stem cell:	n/a	chr7:5609833-5609843
19	CHD2	chr7:5609662-5610178	K562	blood:	n/a	chr7:5609833-5609843
20	CHD2	chr7:5610274-5610423	GM12878	blood:	n/a	n/a
21	CHD2	chr7:5609674-5610073	GM12878	blood:	n/a	chr7:5609833-5609843
22	CHD2	chr7:5609059-5609105	GM12878	blood:	n/a	n/a
23	CHD2	chr7:5609072-5610099	Hela-S3	cervix:	n/a	chr7:5609833-5609843
24	CREB1	chr7:5609480-5610120	H1-hESC	embryonic stem cell:	n/a	n/a
25	CREB1	chr7:5609510-5610254	A549	lung:	n/a	n/a
26	CTCF	chr7:5609640-5609790	HEK293	kidney:	n/a	n/a
27	CTCF	chr7:5609620-5609770	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr7:5609880-5610030	HUVEC	blood vessel:	n/a	chr7:5609970-5609979 chr7:5609907-5609917
29	CTCF	chr7:5609670-5609762	GM10266	blood:	n/a	n/a
30	CTCF	chr7:5609900-5610050	SK-N-SH_RA	brain:	n/a	chr7:5609970-5609979 chr7:5609907-5609917
31	CTCF	chr7:5610280-5610430	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr7:5609060-5609210	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr7:5609540-5609690	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr7:5609520-5609670	NHEK	skin:	n/a	n/a
35	CTCF	chr7:5609540-5609690	BJ	skin:	n/a	n/a
36	CTCF	chr7:5609162-5609181	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr7:5609701-5609727	GM12891	blood:	n/a	n/a
38	CTCF	chr7:5609678-5609712	GM19238	blood:	n/a	n/a
39	CTCF	chr7:5609798-5610113	K562	blood:	n/a	chr7:5609970-5609979 chr7:5609907-5609917
40	CTCF	chr7:5609360-5609510	Caco-2	colon:	n/a	n/a
41	CTCF	chr7:5609660-5609810	GM12873	blood:	n/a	n/a
42	CTCF	chr7:5609560-5609710	GM12870	blood:	n/a	n/a
43	CTCF	chr7:5609620-5609770	GM12865	blood:	n/a	n/a
44	CTCF	chr7:5609654-5609726	GM12892	blood:	n/a	n/a
45	CTCF	chr7:5609920-5610070	GM12875	blood:	n/a	chr7:5609970-5609979
46	CTCF	chr7:5609560-5609710	GM06990	blood:	n/a	n/a
47	CTCF	chr7:5609150-5609157	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr7:5609145-5609146	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr7:5609640-5609790	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr7:5609600-5609750	GM12864	blood:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:5608879-5608929	HPAEpiC	pulmonary alveolar:	n/a
2	chr7:5608879-5608929	HPAEpiC	pulmonary alveolar:	n/a
3	chr7:5609897-5609947	HRE	kidney:	n/a
4	chr7:5609897-5609947	SK-N-SH_RA	brain:	n/a
5	chr7:5609731-5609781	HAEpiC	amniotic membrane:	n/a
6	chr7:5610264-5610314	HepG2	liver:	n/a
7	chr7:5609897-5609947	NT2-D1	testis:	n/a
8	chr7:5609731-5609781	GM19239	blood:	n/a
9	chr7:5609897-5609947	PFSK-1	brain:	n/a
10	chr7:5609897-5609947	HRCEpiC	kidney:	n/a
11	chr7:5610264-5610314	HAEpiC	amniotic membrane:	n/a
12	chr7:5610264-5610314	A549	lung:	n/a
13	chr7:5610264-5610314	SK-N-SH_RA	brain:	n/a
14	chr7:5610264-5610314	MCF-7	breast:	n/a
15	chr7:5609897-5609947	HL-60	blood:	n/a
16	chr7:5609731-5609781	GM12892	blood:	n/a
17	chr7:5608879-5608929	Caco-2	colon:	n/a
18	chr7:5608879-5608929	NHDF-neo	bronchial:	n/a
19	chr7:5609897-5609947	U87	brain:	n/a
20	chr7:5610264-5610314	Jurkat	blood:	n/a
21	chr7:5610264-5610314	AG09319	gingival:	n/a
22	chr7:5609897-5609947	AG04449	skin:	fetal
23	chr7:5609731-5609781	MCF-7	breast:	n/a
24	chr7:5609731-5609781	HRPEpiC	eye:	n/a
25	chr7:5609897-5609947	HCPEpiC	choroid plexus:	n/a
26	chr7:5608879-5608929	GM06990	blood:	n/a
27	chr7:5609731-5609781	HEEpiC	esophagus:	n/a
28	chr7:5609731-5609781	Hepatocyte	liver:	n/a
29	chr7:5609731-5609781	AG04450	lung:	fetal
30	chr7:5609731-5609781	HNPCEpiC	eye:	n/a
31	chr7:5609897-5609947	Caco-2	colon:	n/a
32	chr7:5610264-5610314	HCPEpiC	choroid plexus:	n/a
33	chr7:5609897-5609947	IMR90	lung:	fetal
34	chr7:5610264-5610314	HIPEpiC	eye:	n/a
35	chr7:5608879-5608929	ProgFib	skin:	n/a
36	chr7:5609731-5609781	Hela-S3	cervix:	n/a
37	chr7:5608879-5608929	GM12892	blood:	n/a
38	chr7:5608879-5608929	K562	blood:	n/a
39	chr7:5609731-5609781	Jurkat	blood:	n/a
40	chr7:5610264-5610314	GM12892	blood:	n/a
41	chr7:5609731-5609781	SKMC	muscle:	n/a
42	chr7:5608879-5608929	HAEpiC	amniotic membrane:	n/a
43	chr7:5608879-5608929	BE2_C	brain:	n/a
44	chr7:5609731-5609781	LNCaP	prostate:	n/a
45	chr7:5610264-5610314	HL-60	blood:	n/a
46	chr7:5608879-5608929	T-47D	breast:	n/a
47	chr7:5609897-5609947	NH-A	brain:	n/a
48	chr7:5610264-5610314	ProgFib	skin:	n/a
49	chr7:5608879-5608929	GM19239	blood:	n/a
50	chr7:5609731-5609781	NHDF-neo	bronchial:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:5608955..5610946-chr7:5632329..5633950,2	MCF-7	breast:
2	chr7:5607347..5609764-chr7:5625302..5626880,2	MCF-7	breast:
3	chr17:27720427..27721063-chr7:5609368..5610139,2	Hela-S3	cervix:
4	chr11:62608655..62609595-chr7:5609151..5609926,2	Hela-S3	cervix:
5	chr7:5609119..5611676-chr7:5612260..5613810,2	MCF-7	breast:
6	chr7:5569812..5572018-chr7:5607742..5609745,2	MCF-7	breast:
7	chr7:5508232..5509825-chr7:5608732..5611658,2	MCF-7	breast:
8	chr7:5594823..5597043-chr7:5604963..5607865,2	MCF-7	breast:
9	chr7:5608695..5611336-chr7:5618694..5620634,2	MCF-7	breast:
10	chr7:5600360..5604967-chr7:5605162..5611387,11	MCF-7	breast:
11	chr7:5601903..5606389-chr7:5607716..5610535,5	MCF-7	breast:
12	chr7:5608590..5611609-chr7:5612430..5616441,5	K562	blood:
13	chr7:5609187..5611309-chr7:5612537..5614699,4	MCF-7	breast:
14	chr7:5569738..5572618-chr7:5609274..5610826,2	MCF-7	breast:
15	chr7:5607571..5611303-chr7:5630699..5633841,5	MCF-7	breast:
16	chr7:5610379..5612881-chr7:5704226..5706275,2	K562	blood:

No data

Variant related genes	Relation type
ACTB	TF binding region
ACTB	CpG island
ENSG00000228974	chromatin interactions
ENSG00000075618	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000272719	chromatin interactions
ENSG00000075624	chromatin interactions

Extended variants
information (count: 195 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:195 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368426083	chr7:5607387-5607388	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs113491566	chr7:5607417-5607418	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs543529625	chr7:5607421-5607422	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs555317380	chr7:5607431-5607432	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs573982963	chr7:5607470-5607471	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs190769261	chr7:5607517-5607518	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs567078593	chr7:5607536-5607537	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs182949952	chr7:5607566-5607567	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs562407705	chr7:5607595-5607596	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs73049019	chr7:5607605-5607606	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs563888219	chr7:5607619-5607620	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs531406918	chr7:5607640-5607641	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs376444781	chr7:5607647-5607648	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs150864042	chr7:5607666-5607667	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs138030572	chr7:5607709-5607710	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs571610908	chr7:5607722-5607723	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs528923357	chr7:5607759-5607760	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs547668491	chr7:5607764-5607765	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs565791701	chr7:5607776-5607777	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs143664361	chr7:5607786-5607787	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs532130970	chr7:5607796-5607797	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs3857755	chr7:5607884-5607885	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs567643876	chr7:5607897-5607898	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs852503	chr7:5607908-5607909	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs537129098	chr7:5607916-5607917	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs10279099	chr7:5607923-5607924	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs185671193	chr7:5607962-5607963	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs852502	chr7:5607999-5608000	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs190132604	chr7:5608033-5608034	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs114149112	chr7:5608041-5608042	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs183231808	chr7:5608049-5608050	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs10238674	chr7:5608056-5608057	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs35683134	chr7:5608078-5608079	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs575944822	chr7:5608097-5608098	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs187766271	chr7:5608120-5608121	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs561680345	chr7:5608129-5608130	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs567848910	chr7:5608168-5608169	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs10279453	chr7:5608184-5608185	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs528988682	chr7:5608213-5608214	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs61710459	chr7:5608222-5608223	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs559317814	chr7:5608266-5608267	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs852501	chr7:5608274-5608275	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs551293467	chr7:5608280-5608281	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs569504230	chr7:5608284-5608285	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs577951438	chr7:5608302-5608303	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs115145592	chr7:5608303-5608304	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs549163794	chr7:5608338-5608339	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs529531798	chr7:5608343-5608344	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs192642433	chr7:5608379-5608380	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs184038163	chr7:5608386-5608387	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	22522925	CNVD
Gastric cancer	22014070	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:573 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5603200-5609000	Weak transcription	Fetal Heart	heart
2	chr7:5603400-5607400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr7:5603400-5607600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr7:5603400-5607600	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr7:5603400-5607600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr7:5603400-5607600	Weak transcription	Primary T cells from cord blood	blood
7	chr7:5603400-5608600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr7:5603400-5608600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr7:5603400-5608800	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr7:5603400-5608800	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr7:5603400-5608800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr7:5603400-5608800	Weak transcription	Primary hematopoietic stem cells	blood
13	chr7:5603400-5608800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr7:5603400-5608800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr7:5603400-5608800	Weak transcription	HMEC	breast
16	chr7:5603400-5609000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr7:5603400-5609000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr7:5603400-5609000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr7:5603400-5609000	Weak transcription	Liver	Liver
20	chr7:5603400-5609000	Weak transcription	Brain Angular Gyrus	brain
21	chr7:5603400-5609000	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr7:5603400-5609000	Weak transcription	Left Ventricle	heart
23	chr7:5603400-5609000	Weak transcription	Ovary	ovary
24	chr7:5603400-5609000	Weak transcription	Psoas Muscle	Psoas
25	chr7:5603400-5609000	Weak transcription	Right Atrium	heart
26	chr7:5603400-5609000	Weak transcription	Spleen	Spleen
27	chr7:5603400-5609000	Weak transcription	HSMMtube	muscle
28	chr7:5603400-5609000	Weak transcription	NH-A	brain
29	chr7:5603400-5609000	Weak transcription	NHDF-Ad	bronchial
30	chr7:5603400-5609000	Weak transcription	NHLF	lung
31	chr7:5603600-5607400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr7:5603600-5607400	Weak transcription	Primary T helper cells PMA-I stimulated	--
33	chr7:5603600-5607400	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr7:5603600-5607400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
35	chr7:5603600-5607400	Weak transcription	Fetal Thymus	thymus
36	chr7:5603600-5607400	Weak transcription	Dnd41	blood
37	chr7:5603600-5607600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr7:5603600-5607600	Weak transcription	Fetal Intestine Large	intestine
39	chr7:5603600-5608600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
40	chr7:5603600-5608600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr7:5603600-5608800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr7:5603600-5608800	Weak transcription	Primary B cells from peripheral blood	blood
43	chr7:5603600-5608800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr7:5603600-5608800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr7:5603600-5608800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr7:5603600-5608800	Weak transcription	Adipose Nuclei	Adipose
47	chr7:5603600-5608800	Weak transcription	Brain Hippocampus Middle	brain
48	chr7:5603600-5608800	Weak transcription	Fetal Brain Male	brain
49	chr7:5603600-5608800	Weak transcription	Fetal Stomach	stomach
50	chr7:5603600-5608800	Weak transcription	Hela-S3	cervix

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