Variant report

Variant	nsv887794
Chromosome Location	chr7:17401027-17472677
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:896)
CpG islands
(count:305)
Chromatin interactive
region (count:12)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:896 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:17472514-17472766	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:17445379-17445887	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:17448110-17448897	HepG2	liver:	n/a	chr7:17448501-17448517 chr7:17448542-17448558
4	ATF1	chr7:17448210-17448478	K562	blood:	n/a	n/a
5	ATF1	chr7:17409719-17409918	K562	blood:	n/a	n/a
6	ATF2	chr7:17441733-17443058	GM12878	blood:	n/a	n/a
7	ATF2	chr7:17441580-17443072	GM12878	blood:	n/a	n/a
8	ATF3	chr7:17448179-17448455	K562	blood:	n/a	n/a
9	ATF3	chr7:17448026-17448559	A549	lung:	n/a	n/a
10	ATF3	chr7:17445259-17445891	A549	lung:	n/a	n/a
11	ATF3	chr7:17445307-17445887	A549	lung:	n/a	n/a
12	ATF3	chr7:17448027-17448500	A549	lung:	n/a	n/a
13	BACH1	chr7:17402205-17402446	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr7:17442479-17442964	GM12878	blood:	n/a	n/a
15	BATF	chr7:17422150-17422561	GM12878	blood:	n/a	n/a
16	BATF	chr7:17441907-17442179	GM12878	blood:	n/a	n/a
17	BATF	chr7:17441849-17442266	GM12878	blood:	n/a	n/a
18	BATF	chr7:17442276-17443012	GM12878	blood:	n/a	n/a
19	BCL11A	chr7:17442511-17442916	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:17442448-17443004	GM12878	blood:	n/a	n/a
21	BCL11A	chr7:17413892-17414195	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:17441763-17442232	GM12878	blood:	n/a	chr7:17441972-17441981 chr7:17441975-17441984
23	BCL11A	chr7:17441853-17442099	GM12878	blood:	n/a	chr7:17441972-17441981 chr7:17441975-17441984
24	BCL3	chr7:17445311-17445931	A549	lung:	n/a	n/a
25	BCL3	chr7:17445232-17446030	A549	lung:	n/a	n/a
26	BCL3	chr7:17411033-17411750	A549	lung:	n/a	chr7:17411453-17411462 chr7:17411452-17411461
27	BCL3	chr7:17447908-17448923	A549	lung:	n/a	n/a
28	BCL3	chr7:17448049-17448523	A549	lung:	n/a	n/a
29	BCLAF1	chr7:17441653-17442952	GM12878	blood:	n/a	chr7:17441972-17441981 chr7:17441975-17441984
30	BCLAF1	chr7:17442133-17442966	GM12878	blood:	n/a	n/a
31	BHLHE40	chr7:17422034-17422035	GM12878	blood:	n/a	n/a
32	BHLHE40	chr7:17445375-17445784	HepG2	liver:	n/a	n/a
33	BHLHE40	chr7:17451423-17451834	GM12878	blood:	n/a	n/a
34	BHLHE40	chr7:17448186-17448464	HepG2	liver:	n/a	n/a
35	BHLHE40	chr7:17441635-17443028	GM12878	blood:	n/a	n/a
36	BHLHE40	chr7:17411878-17412262	A549	lung:	n/a	n/a
37	BHLHE40	chr7:17445304-17445710	A549	lung:	n/a	n/a
38	BHLHE40	chr7:17409712-17409938	K562	blood:	n/a	n/a
39	BHLHE40	chr7:17413746-17414159	GM12878	blood:	n/a	n/a
40	BHLHE40	chr7:17439507-17439764	GM12878	blood:	n/a	n/a
41	BRCA1	chr7:17445429-17445936	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr7:17448075-17448667	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr7:17410903-17412330	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr7:17446371-17446826	Hela-S3	cervix:	n/a	n/a
45	CBX3	chr7:17447998-17448665	HCT-116	colon:	n/a	n/a
46	CBX3	chr7:17434201-17434505	K562	blood:	n/a	n/a
47	CBX3	chr7:17402146-17402486	K562	blood:	n/a	n/a
48	CBX3	chr7:17445320-17445880	HCT-116	colon:	n/a	n/a
49	CBX3	chr7:17448004-17448590	HCT-116	colon:	n/a	n/a
50	CBX3	chr7:17411166-17412274	HCT-116	colon:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:17408595-17408645	GM06990	blood:	n/a
2	chr7:17460742-17460792	AoSMC	blood vessel:	n/a
3	chr7:17424006-17424056	AG09309	skin:	n/a
4	chr7:17424006-17424056	HUVEC	blood vessel:	n/a
5	chr7:17402192-17402242	PrEC	prostate:	n/a
6	chr7:17460742-17460792	SAEC	small airway:	n/a
7	chr7:17402192-17402242	HCPEpiC	choroid plexus:	n/a
8	chr7:17424006-17424056	GM19239	blood:	n/a
9	chr7:17408595-17408645	NHBE	bronchial:	n/a
10	chr7:17408595-17408645	LNCaP	prostate:	n/a
11	chr7:17460742-17460792	AG04450	lung:	fetal
12	chr7:17402192-17402242	T-47D	breast:	n/a
13	chr7:17460742-17460792	HEEpiC	esophagus:	n/a
14	chr7:17402192-17402242	Jurkat	blood:	n/a
15	chr7:17424006-17424056	AoSMC	blood vessel:	n/a
16	chr7:17410340-17410390	AG09309	skin:	n/a
17	chr7:17410340-17410390	T-47D	breast:	n/a
18	chr7:17408595-17408645	MCF10A-Er-Src	breast:	n/a
19	chr7:17460742-17460792	A549	lung:	n/a
20	chr7:17402192-17402242	AG10803	skin:	n/a
21	chr7:17460742-17460792	HUVEC	blood vessel:	n/a
22	chr7:17410340-17410390	HepG2	liver:	n/a
23	chr7:17408595-17408645	SAEC	small airway:	n/a
24	chr7:17402192-17402242	ECC-1	luminal epithelium:	n/a
25	chr7:17410340-17410390	HIPEpiC	eye:	n/a
26	chr7:17424006-17424056	HCT-116	colon:	n/a
27	chr7:17460742-17460792	GM12878	blood:	n/a
28	chr7:17402192-17402242	SK-N-SH	brain:	n/a
29	chr7:17410340-17410390	U87	brain:	n/a
30	chr7:17410340-17410390	Hepatocyte	liver:	n/a
31	chr7:17408595-17408645	HCT-116	colon:	n/a
32	chr7:17408595-17408645	AG09319	gingival:	n/a
33	chr7:17408595-17408645	PFSK-1	brain:	n/a
34	chr7:17424006-17424056	U87	brain:	n/a
35	chr7:17460742-17460792	Caco-2	colon:	n/a
36	chr7:17410340-17410390	A549	lung:	n/a
37	chr7:17408595-17408645	BE2_C	brain:	n/a
38	chr7:17424006-17424056	PANC-1	pancreas:	n/a
39	chr7:17424006-17424056	GM12878	blood:	n/a
40	chr7:17410340-17410390	MCF10A-Er-Src	breast:	n/a
41	chr7:17460742-17460792	HCT-116	colon:	n/a
42	chr7:17410340-17410390	BJ	skin:	n/a
43	chr7:17408595-17408645	AG04450	lung:	fetal
44	chr7:17460742-17460792	HPAEpiC	pulmonary alveolar:	n/a
45	chr7:17460742-17460792	HRPEpiC	eye:	n/a
46	chr7:17410340-17410390	BE2_C	brain:	n/a
47	chr7:17424006-17424056	ovcar-3	ovarian:	n/a
48	chr7:17410340-17410390	GM12878	blood:	n/a
49	chr7:17410340-17410390	HNPCEpiC	eye:	n/a
50	chr7:17402192-17402242	H1-hESC	embryonic stem cell:	embryo

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:17385888..17388096-chr7:17407942..17409805,2	MCF-7	breast:
2	chr7:17469734..17471826-chr7:17488594..17490473,2	MCF-7	breast:
3	chr7:17394503..17397542-chr7:17400544..17403878,3	K562	blood:
4	chr7:17402053..17404389-chr7:17408821..17410767,2	MCF-7	breast:
5	chr7:17402053..17404389-chr7:17408821..17410767,2	MCF-7	breast:
6	chr7:17393956..17396840-chr7:17402378..17404335,2	K562	blood:
7	chr7:17338744..17341559-chr7:17444382..17446981,2	MCF-7	breast:
8	chr7:17411899..17413938-chr7:17417894..17419899,4	MCF-7	breast:
9	chr7:17349709..17351972-chr7:17405529..17407075,2	MCF-7	breast:
10	chr7:17448128..17449838-chr7:17451617..17454336,2	MCF-7	breast:
11	chr7:17448128..17449838-chr7:17451617..17454336,2	MCF-7	breast:
12	chr7:17398384..17399980-chr7:17400183..17402691,2	K562	blood:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNX13-5	chr7:17463483-17463741	l_3367_chr7:17380930-17457210_prostate
2	lnc-SNX13-4	chr7:17471319-17471375	l_3368_chr7:17469554-17530296_testes
3	lnc-SNX13-5	chr7:17442179-17442382	NONHSAT119332
4	lnc-AHR-1	chr7:17414541-17414679	NR_110014
5	lnc-AHR-1	chr7:17414491-17414679	ENSG00000236318
6	lnc-SNX13-5	chr7:17440626-17440649	NONHSAT119331
7	lnc-AHR-4	chr7:17472301-17472813	NONHSAT119328
8	lnc-SNX13-5	chr7:17441622-17442386	l_3367_chr7:17380930-17457210_prostate
9	lnc-SNX13-5	chr7:17463483-17463585	NONHSAT119332
10	lnc-SNX13-5	chr7:17462831-17462911	NONHSAT119332
11	lnc-AHR-4	chr7:17455030-17455097	NONHSAT119328
12	lnc-SNX13-5	chr7:17462827-17462911	NONHSAT119331
13	lnc-SNX13-5	chr7:17462827-17462911	l_3367_chr7:17380930-17457210_prostate
14	lnc-SNX13-5	chr7:17466631-17466821	NONHSAT119331
15	lnc-SNX13-5	chr7:17457149-17457210	l_3367_chr7:17380930-17457210_prostate
16	lnc-SNX13-4	chr7:17469594-17469691	NONHSAT119333
17	lnc-SNX13-5	chr7:17441097-17441254	NONHSAT119331
18	lnc-SNX13-4	chr7:17471319-17471375	NONHSAT119333
19	lnc-SNX13-4	chr7:17469555-17469691	l_3368_chr7:17469554-17530296_testes
20	lnc-AHR-4	chr7:17457144-17457210	NONHSAT119328
21	lnc-SNX13-5	chr7:17463608-17463738	NONHSAT119331
22	lnc-AHR-1	chr7:17414541-17414679	NR_110015

No data

Variant related genes	Relation type
ENSG00000236318	TF binding region
ENSG00000199473	TF binding region
ENSG00000236318	CpG island
ENSG00000199473	CpG island
ENSG00000199473	chromatin interactions
ENSG00000237773	chromatin interactions

Extended variants
information (count: 3035 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:3035 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7791070	chr7:17401027-17401028	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs558312204	chr7:17401092-17401093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs149180555	chr7:17401110-17401111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs118042827	chr7:17401120-17401121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs571336737	chr7:17401125-17401126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs545755438	chr7:17401213-17401214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs117986557	chr7:17401244-17401245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs138850784	chr7:17401245-17401246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs528066271	chr7:17401281-17401282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs192661735	chr7:17401321-17401322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs561450270	chr7:17401329-17401330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs184313448	chr7:17401332-17401333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs551169839	chr7:17401349-17401350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs569336588	chr7:17401388-17401389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs146817986	chr7:17401539-17401540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs538612139	chr7:17401561-17401562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs1074043	chr7:17401573-17401574	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs368561106	chr7:17401613-17401614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554253587	chr7:17401752-17401753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs534195260	chr7:17401782-17401783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555754634	chr7:17401815-17401816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs567784383	chr7:17401827-17401828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs571715052	chr7:17401843-17401844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs574161898	chr7:17401850-17401851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs537920691	chr7:17401899-17401900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs113434203	chr7:17401908-17401909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs557157849	chr7:17401993-17401994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs374540382	chr7:17402025-17402026	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs575340833	chr7:17402027-17402028	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs546116438	chr7:17402035-17402036	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs557774921	chr7:17402038-17402039	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs139222263	chr7:17402041-17402042	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs539864063	chr7:17402042-17402043	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs188655207	chr7:17402059-17402060	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs200636203	chr7:17402068-17402069	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs528988414	chr7:17402077-17402078	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs543951566	chr7:17402090-17402091	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs181603424	chr7:17402101-17402102	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs533354705	chr7:17402118-17402119	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs551912204	chr7:17402129-17402130	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs376423334	chr7:17402144-17402145	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs527963313	chr7:17402152-17402153	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs549416502	chr7:17402193-17402194	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs567652002	chr7:17402195-17402196	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs538380664	chr7:17402210-17402211	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs556370672	chr7:17402218-17402219	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs571672838	chr7:17402228-17402229	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs540492178	chr7:17402238-17402239	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs143355969	chr7:17402242-17402243	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs557500489	chr7:17402247-17402248	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Melanoma	18172304	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Bladder cancer	21909424	CNVD
Cancer	21183584	CNVD
Autism	20808228	CNVD
Sezary syndrome	18413736	CNVD
Autism	22495309	CNVD
Depressive disorder	21152026	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:595 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:17356200-17409400	Weak transcription	Pancreas	Pancrea
2	chr7:17379600-17408600	Weak transcription	Small Intestine	intestine
3	chr7:17379800-17407400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr7:17380000-17402000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr7:17380000-17405000	Weak transcription	Primary T cells from cord blood	blood
6	chr7:17380000-17409400	Weak transcription	Rectal Smooth Muscle	rectum
7	chr7:17380000-17411000	Weak transcription	Aorta	Aorta
8	chr7:17380200-17408800	Weak transcription	A549	lung
9	chr7:17381200-17407200	Weak transcription	NH-A	brain
10	chr7:17382800-17408800	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr7:17383000-17408800	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr7:17383800-17407200	Weak transcription	NHDF-Ad	bronchial
13	chr7:17386800-17404600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr7:17387200-17406800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr7:17387400-17406800	Weak transcription	Osteobl	bone
16	chr7:17387800-17406800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr7:17388200-17408600	Weak transcription	HSMM	muscle
18	chr7:17390800-17407000	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr7:17394400-17407200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr7:17398000-17405400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr7:17398000-17407600	Weak transcription	Left Ventricle	heart
22	chr7:17398200-17407600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr7:17399000-17408600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr7:17399600-17407200	Weak transcription	HSMMtube	muscle
25	chr7:17399600-17407600	Weak transcription	Lung	lung
26	chr7:17400600-17407400	Weak transcription	Fetal Lung	lung
27	chr7:17401000-17402600	Enhancers	Fetal Stomach	stomach
28	chr7:17402000-17402600	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr7:17402200-17402600	Enhancers	NHLF	lung
30	chr7:17402400-17402800	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr7:17402600-17407400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr7:17402600-17407400	Weak transcription	NHLF	lung
33	chr7:17402800-17407600	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr7:17403600-17404400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr7:17403600-17407400	Weak transcription	Ovary	ovary
36	chr7:17404400-17404600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr7:17404600-17406000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
38	chr7:17404600-17410800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr7:17405000-17406000	Enhancers	Primary T cells from cord blood	blood
40	chr7:17405400-17405800	Enhancers	Primary T helper cells PMA-I stimulated	--
41	chr7:17405400-17405800	Enhancers	Primary T helper cells fromperipheralblood	blood
42	chr7:17405400-17406000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr7:17405400-17408600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr7:17405600-17406000	Enhancers	HMEC	breast
45	chr7:17405600-17406000	Enhancers	NHEK	skin
46	chr7:17405600-17408800	Weak transcription	Fetal Intestine Small	intestine
47	chr7:17406000-17407200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr7:17406000-17407600	Weak transcription	NHEK	skin
49	chr7:17406000-17408400	Weak transcription	HMEC	breast
50	chr7:17406600-17409000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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