Variant report

Variant	esv1802979
Chromosome Location	chr7:17816528-17908546
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:393)
CpG islands
(count:183)
Chromatin interactive
region (count:39)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:393 , 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	chr7:17855043-17855259	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:17853694-17854015	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:17821787-17821810	K562	blood:	n/a	n/a
4	ATF3	chr7:17854938-17855347	HepG2	liver:	n/a	n/a
5	BACH1	chr7:17846859-17846996	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr7:17898844-17899093	GM12878	blood:	n/a	n/a
7	BATF	chr7:17883700-17883943	GM12878	blood:	n/a	n/a
8	BATF	chr7:17883672-17883959	GM12878	blood:	n/a	n/a
9	BATF	chr7:17871903-17872115	GM12878	blood:	n/a	chr7:17871948-17871957
10	BATF	chr7:17894938-17895167	GM12878	blood:	n/a	n/a
11	BATF	chr7:17894349-17894613	GM12878	blood:	n/a	n/a
12	BATF	chr7:17898772-17899044	GM12878	blood:	n/a	n/a
13	BATF	chr7:17871956-17872120	GM12878	blood:	n/a	n/a
14	BATF	chr7:17894311-17894607	GM12878	blood:	n/a	n/a
15	CBX3	chr7:17846956-17847377	K562	blood:	n/a	n/a
16	CEBPB	chr7:17847113-17847242	K562	blood:	n/a	n/a
17	CEBPB	chr7:17855038-17855296	H1-hESC	embryonic stem cell:	n/a	chr7:17855158-17855169
18	CEBPB	chr7:17855104-17855278	Hela-S3	cervix:	n/a	chr7:17855158-17855169
19	CEBPB	chr7:17841714-17841939	A549	lung:	n/a	chr7:17841865-17841876
20	CEBPB	chr7:17869943-17870075	HepG2	liver:	n/a	chr7:17870003-17870016 chr7:17869968-17869985
21	CEBPB	chr7:17855000-17855339	HepG2	liver:	n/a	chr7:17855158-17855169
22	CEBPB	chr7:17854910-17855278	HepG2	liver:	n/a	chr7:17855158-17855169
23	CEBPB	chr7:17841856-17841895	Hela-S3	cervix:	n/a	chr7:17841865-17841876
24	CEBPB	chr7:17854993-17855308	MCF-7	breast:	n/a	chr7:17855158-17855169
25	CEBPB	chr7:17838431-17838630	K562	blood:	n/a	chr7:17838551-17838564 chr7:17838551-17838564
26	CEBPB	chr7:17841743-17841975	HepG2	liver:	n/a	chr7:17841865-17841876
27	CEBPB	chr7:17854993-17855267	HepG2	liver:	n/a	chr7:17855158-17855169
28	CEBPB	chr7:17869897-17870122	Hela-S3	cervix:	n/a	chr7:17870003-17870016 chr7:17869968-17869985
29	CEBPB	chr7:17855019-17855320	HepG2	liver:	n/a	chr7:17855158-17855169
30	CEBPB	chr7:17855070-17855232	A549	lung:	n/a	chr7:17855158-17855169
31	CEBPB	chr7:17841706-17842004	IMR90	lung:	n/a	chr7:17841865-17841876
32	CEBPB	chr7:17854952-17855320	MCF-7	breast:	n/a	chr7:17855158-17855169
33	CEBPD	chr7:17854887-17855229	HepG2	liver:	n/a	n/a
34	CHD2	chr7:17846770-17847089	K562	blood:	n/a	n/a
35	CHD2	chr7:17846803-17847058	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr7:17901580-17901730	GM06990	blood:	n/a	n/a
37	CTCF	chr7:17821260-17821410	AG09309	skin:	n/a	n/a
38	CTCF	chr7:17901500-17901735	GM12878	blood:	n/a	n/a
39	CTCF	chr7:17901600-17901750	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr7:17821240-17821390	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr7:17821606-17821611	Gliobla	brain:	n/a	n/a
42	CTCF	chr7:17828840-17828990	GM12866	blood:	n/a	n/a
43	CTCF	chr7:17901580-17901730	BE2_C	brain:	n/a	n/a
44	CTCF	chr7:17847401-17847428	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr7:17903420-17903570	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr7:17821280-17821430	AoAF	blood vessel:	n/a	n/a
47	CTCF	chr7:17903520-17903670	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr7:17903574-17903643	Medullo	brain:	n/a	n/a
49	CTCF	chr7:17901635-17901660	GM12878	blood:	n/a	n/a
50	CTCF	chr7:17821360-17821510	HPAF	blood vessel:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:17822217-17822267	T-47D	breast:	n/a
2	chr7:17831714-17831764	AG04450	lung:	fetal
3	chr7:17822217-17822267	HRE	kidney:	n/a
4	chr7:17831714-17831764	AG09319	gingival:	n/a
5	chr7:17826367-17826417	GM12878	blood:	n/a
6	chr7:17831714-17831764	HNPCEpiC	eye:	n/a
7	chr7:17826367-17826417	HEK293	kidney:	embryo
8	chr7:17831714-17831764	GM12891	blood:	n/a
9	chr7:17822217-17822267	HNPCEpiC	eye:	n/a
10	chr7:17826367-17826417	PANC-1	pancreas:	n/a
11	chr7:17831714-17831764	HL-60	blood:	n/a
12	chr7:17826367-17826417	GM19239	blood:	n/a
13	chr7:17826367-17826417	AG09309	skin:	n/a
14	chr7:17822217-17822267	HCM	heart:	n/a
15	chr7:17822217-17822267	RPTEC	kidney:	n/a
16	chr7:17831714-17831764	HPAEpiC	pulmonary alveolar:	n/a
17	chr7:17822217-17822267	AG04450	lung:	fetal
18	chr7:17831714-17831764	AG10803	skin:	n/a
19	chr7:17831714-17831764	A549	lung:	n/a
20	chr7:17826367-17826417	MCF-7	breast:	n/a
21	chr7:17831714-17831764	HCF	heart:	n/a
22	chr7:17822217-17822267	SK-N-SH	brain:	n/a
23	chr7:17826367-17826417	NHDF-neo	bronchial:	n/a
24	chr7:17826367-17826417	ProgFib	skin:	n/a
25	chr7:17822217-17822267	GM19239	blood:	n/a
26	chr7:17831714-17831764	NHDF-neo	bronchial:	n/a
27	chr7:17831714-17831764	SK-N-SH_RA	brain:	n/a
28	chr7:17831714-17831764	ProgFib	skin:	n/a
29	chr7:17831714-17831764	AG04449	skin:	fetal
30	chr7:17826367-17826417	BE2_C	brain:	n/a
31	chr7:17826367-17826417	NHBE	bronchial:	n/a
32	chr7:17831714-17831764	HMEC	breast:	n/a
33	chr7:17826367-17826417	NB4	blood:	n/a
34	chr7:17826367-17826417	K562	blood:	n/a
35	chr7:17822217-17822267	GM12878	blood:	n/a
36	chr7:17822217-17822267	BJ	skin:	n/a
37	chr7:17831714-17831764	BJ	skin:	n/a
38	chr7:17826367-17826417	SKMC	muscle:	n/a
39	chr7:17831714-17831764	PrEC	prostate:	n/a
40	chr7:17826367-17826417	HepG2	liver:	n/a
41	chr7:17826367-17826417	HRCEpiC	kidney:	n/a
42	chr7:17822217-17822267	CMK	blood:	n/a
43	chr7:17822217-17822267	Hela-S3	cervix:	n/a
44	chr7:17826367-17826417	U87	brain:	n/a
45	chr7:17826367-17826417	AG04449	skin:	fetal
46	chr7:17826367-17826417	A549	lung:	n/a
47	chr7:17826367-17826417	BJ	skin:	n/a
48	chr7:17822217-17822267	LNCaP	prostate:	n/a
49	chr7:17826367-17826417	HL-60	blood:	n/a
50	chr7:17831714-17831764	HepG2	liver:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:17840712..17842698-chr7:17979227..17982552,3	MCF-7	breast:
2	chr7:17829280..17831283-chr7:17835697..17837635,2	K562	blood:
3	chr7:17886526..17888087-chr7:17888537..17890269,2	MCF-7	breast:
4	chr7:17861690..17863309-chr7:17878312..17881070,2	K562	blood:
5	chr7:17901839..17903435-chr7:17980572..17982643,2	MCF-7	breast:
6	chr7:17837121..17839651-chr7:17841866..17844504,2	K562	blood:
7	chr7:17816362..17819179-chr7:17820951..17822605,2	K562	blood:
8	chr7:17864166..17867586-chr7:17869183..17871409,4	K562	blood:
9	chr7:17868673..17871500-chr7:17873119..17875470,2	K562	blood:
10	chr7:17897387..17900281-chr7:17901948..17903936,2	K562	blood:
11	chr7:17863336..17865666-chr7:17868902..17871409,2	K562	blood:
12	chr7:17853387..17855220-chr7:17856862..17859241,2	K562	blood:
13	chr7:17853678..17855376-chr7:17978755..17981532,2	MCF-7	breast:
14	chr7:17831699..17833248-chr7:17838941..17840682,2	K562	blood:
15	chr5:139045624..139046135-chr7:17821105..17821613,2	HCT-116	colon:
16	chr7:17853768..17855990-chr7:17915652..17917897,2	K562	blood:
17	chr7:17844492..17846186-chr7:17870318..17872913,2	MCF-7	breast:
18	chr7:17886413..17888051-chr7:17895636..17897500,2	MCF-7	breast:
19	chr7:17897387..17900281-chr7:17901948..17903936,2	K562	blood:
20	chr7:17886526..17888087-chr7:17888537..17890269,2	MCF-7	breast:
21	chr7:17882358..17885096-chr7:17950396..17953115,2	K562	blood:
22	chr7:17890085..17891646-chr7:17912028..17913718,2	MCF-7	breast:
23	chr7:17861812..17864316-chr7:17866527..17868627,2	K562	blood:
24	chr7:17831699..17833248-chr7:17838941..17840682,2	K562	blood:
25	chr7:17861690..17863309-chr7:17878312..17881070,2	K562	blood:
26	chr7:17837121..17839651-chr7:17841866..17844504,2	K562	blood:
27	chr7:17863336..17865666-chr7:17868902..17871409,2	K562	blood:
28	chr7:17861812..17864316-chr7:17866527..17868627,2	K562	blood:
29	chr7:17829280..17831283-chr7:17835697..17837635,2	K562	blood:
30	chr7:17865698..17868586-chr7:17873859..17875914,2	K562	blood:
31	chr7:17853387..17855220-chr7:17856862..17859241,2	K562	blood:
32	chr7:17816362..17819179-chr7:17820951..17822605,2	K562	blood:
33	chr7:17865698..17868586-chr7:17873859..17875914,2	K562	blood:
34	chr7:17864166..17867586-chr7:17869183..17871409,4	K562	blood:
35	chr7:17844492..17846186-chr7:17870318..17872913,2	MCF-7	breast:
36	chr7:17868673..17871500-chr7:17873119..17875470,2	K562	blood:
37	chr7:17872510..17875086-chr7:17979395..17981460,2	MCF-7	breast:
38	chr7:17856945..17858744-chr7:17859975..17861675,2	K562	blood:
39	chr7:17886413..17888051-chr7:17895636..17897500,2	MCF-7	breast:

No data

Variant related genes	Relation type
SNX13	TF binding region
SNX13	CpG island
ENSG00000071189	chromatin interactions

Extended variants
information (count: 3517 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:3517 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10227462	chr7:17816528-17816529	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs551129455	chr7:17816540-17816541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs537855767	chr7:17816551-17816552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs74877068	chr7:17816563-17816564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs149303946	chr7:17816589-17816590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs373551394	chr7:17816594-17816595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569774791	chr7:17816638-17816639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2723510	chr7:17816639-17816640	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs201796908	chr7:17816647-17816648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs555489680	chr7:17816702-17816703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572330108	chr7:17816703-17816704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535054453	chr7:17816738-17816739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556606534	chr7:17816780-17816781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs578245999	chr7:17816794-17816795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs2691584	chr7:17816817-17816818	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs577067675	chr7:17816825-17816826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554360724	chr7:17816850-17816851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs55658418	chr7:17816877-17816878	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs542795896	chr7:17816918-17816919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556469376	chr7:17816941-17816942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188644427	chr7:17816954-17816955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs571570903	chr7:17816955-17816956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs115163861	chr7:17816956-17816957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs192341411	chr7:17816978-17816979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35219509	chr7:17816983-17816984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184450252	chr7:17817000-17817001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551161879	chr7:17817005-17817006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566288483	chr7:17817015-17817016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs572299702	chr7:17817018-17817019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs2723509	chr7:17817037-17817038	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs375192463	chr7:17817088-17817089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548851049	chr7:17817137-17817138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs58458725	chr7:17817182-17817183	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs538417435	chr7:17817183-17817184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541923596	chr7:17817186-17817187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs144708401	chr7:17817193-17817194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs148537171	chr7:17817214-17817215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539298801	chr7:17817227-17817228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189601795	chr7:17817300-17817301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182192916	chr7:17817308-17817309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1404421	chr7:17817431-17817432	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs372035890	chr7:17817448-17817449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546586900	chr7:17817468-17817469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554802292	chr7:17817494-17817495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs145493770	chr7:17817551-17817552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527257329	chr7:17817583-17817584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543476229	chr7:17817613-17817614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs116720870	chr7:17817643-17817644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577523271	chr7:17817650-17817651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544940971	chr7:17817661-17817662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
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
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	20531469	CNVD

Chromatin state (count:2031 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:17812400-17846200	Weak transcription	Fetal Stomach	stomach
2	chr7:17812400-17852200	Weak transcription	Esophagus	oesophagus
3	chr7:17812600-17887600	Weak transcription	Gastric	stomach
4	chr7:17813400-17821200	Weak transcription	Thymus	Thymus
5	chr7:17813600-17879200	Weak transcription	HSMMtube	muscle
6	chr7:17813800-17833200	Weak transcription	Fetal Thymus	thymus
7	chr7:17813800-17836200	Weak transcription	HSMM	muscle
8	chr7:17814200-17833200	Weak transcription	Right Ventricle	heart
9	chr7:17814400-17821200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr7:17814600-17828600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr7:17814600-17833400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr7:17815000-17833200	Weak transcription	Left Ventricle	heart
13	chr7:17815200-17829200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr7:17815400-17821000	Weak transcription	NH-A	brain
15	chr7:17816200-17833200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr7:17817400-17887600	Weak transcription	Pancreas	Pancrea
17	chr7:17818200-17821600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr7:17820800-17833200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr7:17821000-17822600	Enhancers	HUVEC	blood vessel
20	chr7:17821000-17822600	Enhancers	NH-A	brain
21	chr7:17821200-17821600	Enhancers	Thymus	Thymus
22	chr7:17821200-17822000	Enhancers	Stomach Mucosa	stomach
23	chr7:17821200-17822400	Enhancers	HMEC	breast
24	chr7:17821200-17823800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr7:17821200-17827000	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr7:17821400-17822400	Enhancers	NHEK	skin
27	chr7:17821400-17822600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr7:17821600-17821800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr7:17821600-17821800	Enhancers	Sigmoid Colon	Sigmoid Colon
30	chr7:17821600-17821800	Weak transcription	Thymus	Thymus
31	chr7:17821600-17822000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr7:17821600-17822000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr7:17821600-17822200	Enhancers	NHLF	lung
34	chr7:17821600-17822400	Enhancers	Osteobl	bone
35	chr7:17821800-17822400	Enhancers	Thymus	Thymus
36	chr7:17821800-17833200	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr7:17821800-17847000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr7:17822000-17846200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr7:17822000-17852600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr7:17822200-17837000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr7:17822200-17845600	Weak transcription	NHLF	lung
42	chr7:17822400-17823400	Weak transcription	NHEK	skin
43	chr7:17822400-17823600	Weak transcription	HMEC	breast
44	chr7:17822400-17826800	Weak transcription	Thymus	Thymus
45	chr7:17822400-17833000	Weak transcription	Osteobl	bone
46	chr7:17822400-17833200	Weak transcription	Fetal Muscle Leg	muscle
47	chr7:17822600-17832800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr7:17822600-17833200	Weak transcription	HUVEC	blood vessel
49	chr7:17822600-17833200	Weak transcription	NH-A	brain
50	chr7:17823000-17846200	Weak transcription	Fetal Intestine Small	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links