Variant report

Variant	esv1793320
Chromosome Location	chr7:102677917-102706209
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:537)
CpG islands
(count:0)
Chromatin interactive
region (count:38)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:537 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102678611-102678721	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:102702422-102702598	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:102692007-102692254	K562	blood:	n/a	n/a
4	ATF1	chr7:102682488-102682513	K562	blood:	n/a	n/a
5	ATF1	chr7:102678614-102678853	K562	blood:	n/a	n/a
6	BHLHE40	chr7:102702515-102702570	GM12878	blood:	n/a	n/a
7	BRCA1	chr7:102702403-102702680	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr7:102689274-102689575	HCT-116	colon:	n/a	n/a
9	CBX3	chr7:102678220-102678790	K562	blood:	n/a	n/a
10	CBX3	chr7:102689242-102689609	K562	blood:	n/a	n/a
11	CBX3	chr7:102677926-102679028	K562	blood:	n/a	n/a
12	CBX3	chr7:102689289-102689621	K562	blood:	n/a	n/a
13	CCNT2	chr7:102678586-102678788	K562	blood:	n/a	n/a
14	CEBPB	chr7:102699917-102700274	IMR90	lung:	n/a	n/a
15	CEBPB	chr7:102696518-102696818	HepG2	liver:	n/a	chr7:102696651-102696662
16	CEBPB	chr7:102684262-102684278	K562	blood:	n/a	n/a
17	CEBPB	chr7:102699930-102700270	HepG2	liver:	n/a	n/a
18	CEBPB	chr7:102696497-102696742	IMR90	lung:	n/a	chr7:102696651-102696662
19	CEBPB	chr7:102696507-102696815	K562	blood:	n/a	chr7:102696651-102696662
20	CEBPB	chr7:102699925-102700270	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr7:102700019-102700235	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr7:102699932-102700227	A549	lung:	n/a	n/a
23	CEBPB	chr7:102699931-102700264	A549	lung:	n/a	n/a
24	CEBPB	chr7:102684238-102684306	A549	lung:	n/a	chr7:102684290-102684301
25	CEBPB	chr7:102678678-102678710	K562	blood:	n/a	n/a
26	CEBPB	chr7:102696535-102696811	A549	lung:	n/a	chr7:102696651-102696662
27	CEBPB	chr7:102699942-102700295	K562	blood:	n/a	n/a
28	CEBPZ	chr7:102689438-102689525	HepG2	liver:	n/a	n/a
29	CHD2	chr7:102678510-102678772	K562	blood:	n/a	n/a
30	CHD2	chr7:102703250-102703334	K562	blood:	n/a	n/a
31	CTCF	chr7:102702480-102702630	NHDF-neo	bronchial:	n/a	n/a
32	CTCF	chr7:102706200-102706350	GM06990	blood:	n/a	n/a
33	CTCF	chr7:102706206-102706427	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr7:102706200-102706350	WERI-Rb-1	eye:	n/a	n/a
35	CTCF	chr7:102706166-102706530	A549	lung:	n/a	n/a
36	CTCF	chr7:102702500-102702650	HPAF	blood vessel:	n/a	chr7:102702642-102702649
37	CTCF	chr7:102704440-102704590	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr7:102688556-102688650	Pancreas_OC	pancreas:	n/a	n/a
39	CTCF	chr7:102702440-102702680	Hela-S3	cervix:	n/a	chr7:102702642-102702649
40	CTCF	chr7:102702480-102702630	HAc	cerebellar:	n/a	n/a
41	CTCF	chr7:102702423-102702662	Lung_OC	lung:	n/a	chr7:102702642-102702649
42	CTCF	chr7:102702451-102702645	GM10266	blood:	n/a	n/a
43	CTCF	chr7:102702460-102702610	GM12871	blood:	n/a	n/a
44	CTCF	chr7:102702480-102702630	AG04449	skin:	n/a	n/a
45	CTCF	chr7:102702363-102702776	MCF-7	breast:	n/a	chr7:102702642-102702649
46	CTCF	chr7:102702500-102702650	HPF	lung:	n/a	chr7:102702642-102702649
47	CTCF	chr7:102691991-102692320	K562	blood:	n/a	n/a
48	CTCF	chr7:102678403-102678445	MCF-7	breast:	n/a	n/a
49	CTCF	chr7:102702460-102702610	AG04450	lung:	n/a	n/a
50	CTCF	chr7:102702500-102702650	HMF	breast:	n/a	chr7:102702642-102702649

No data

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:102683119..102685488-chr7:102687684..102690602,4	K562	blood:
2	chr7:102616376..102618625-chr7:102696676..102699468,2	K562	blood:
3	chr7:102673845..102676724-chr7:102700499..102703034,2	K562	blood:
4	chr7:102692413..102696625-chr7:102698429..102700505,5	K562	blood:
5	chr7:102686325..102688717-chr7:102697230..102700034,3	K562	blood:
6	chr7:102696664..102700307-chr7:102700461..102702793,3	K562	blood:
7	chr7:102704001..102706200-chr7:102714762..102716967,2	K562	blood:
8	chr7:102611388..102613212-chr7:102692044..102694457,2	K562	blood:
9	chr7:102686325..102688717-chr7:102697230..102700034,3	K562	blood:
10	chr7:102694258..102697387-chr7:102697873..102700053,4	K562	blood:
11	chr7:102630195..102631725-chr7:102699498..102701582,2	K562	blood:
12	chr7:102676967..102679361-chr7:102702578..102705004,2	K562	blood:
13	chr7:102696664..102700307-chr7:102700461..102702793,3	K562	blood:
14	chr7:102705659..102708585-chr7:102755906..102758111,2	K562	blood:
15	chr7:102692413..102696625-chr7:102698429..102700505,5	K562	blood:
16	chr7:102608423..102610942-chr7:102700411..102702582,3	K562	blood:
17	chr7:102389656..102391894-chr7:102702213..102705034,2	MCF-7	breast:
18	chr7:102704633..102706824-chr7:102709048..102710835,2	MCF-7	breast:
19	chr7:102700472..102704073-chr7:102705229..102707917,4	K562	blood:
20	chr7:102691392..102694110-chr7:102703544..102706469,2	K562	blood:
21	chr7:102674721..102677676-chr7:102695707..102697752,2	K562	blood:
22	chr7:102629638..102632111-chr7:102696219..102697817,2	K562	blood:
23	chr7:102676967..102679361-chr7:102702578..102705004,2	K562	blood:
24	chr7:102648277..102650266-chr7:102675319..102678268,2	K562	blood:
25	chr7:102670106..102673764-chr7:102674096..102679357,5	K562	blood:
26	chr7:102694258..102697387-chr7:102697873..102700053,4	K562	blood:
27	chr7:102701175..102706120-chr7:102711307..102716730,7	K562	blood:
28	chr7:102612993..102615642-chr7:102682873..102685524,2	K562	blood:
29	chr7:102702765..102704335-chr7:102714764..102716771,2	MCF-7	breast:
30	chr7:102696119..102699764-chr7:102712754..102715415,3	K562	blood:
31	chr7:102611593..102615684-chr7:102700169..102704441,4	K562	blood:
32	chr7:102704923..102706991-chr7:102714522..102716456,2	MCF-7	breast:
33	chr7:102430529..102431497-chr7:102702527..102703245,2	K562	blood:
34	chr7:102691392..102694110-chr7:102703544..102706469,2	K562	blood:
35	chr7:102684811..102686688-chr7:102714755..102716394,2	MCF-7	breast:
36	chr7:102700472..102704073-chr7:102705229..102707917,4	K562	blood:
37	chr7:102618985..102623059-chr7:102696660..102699924,3	K562	blood:
38	chr7:102620399..102622083-chr7:102705547..102707771,2	K562	blood:

No data

Variant related genes	Relation type
FBXL13	TF binding region
ENSG00000236226	chromatin interactions
ENSG00000161040	chromatin interactions
ENSG00000230257	chromatin interactions
ENSG00000222011	chromatin interactions
ENSG00000170632	chromatin interactions

Extended variants
information (count: 1062 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1062 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185718623	chr7:102677940-102677941	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs116118057	chr7:102677994-102677995	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs76105685	chr7:102678014-102678015	Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs200440476	chr7:102678032-102678033	Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs530113349	chr7:102678034-102678035	Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs112137198	chr7:102678082-102678083	Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs547996970	chr7:102678095-102678096	Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs566260717	chr7:102678105-102678106	Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs114644065	chr7:102678114-102678115	Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs192064641	chr7:102678204-102678205	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs569727392	chr7:102678286-102678287	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs146884773	chr7:102678290-102678291	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs558239076	chr7:102678299-102678300	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs115654429	chr7:102678340-102678341	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs540954289	chr7:102678356-102678357	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs140652948	chr7:102678388-102678389	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs574291279	chr7:102678410-102678411	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs13221585	chr7:102678422-102678423	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs561054386	chr7:102678457-102678458	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs562433034	chr7:102678467-102678468	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs543818830	chr7:102678474-102678475	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs373048295	chr7:102678496-102678497	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs529734783	chr7:102678513-102678514	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs565112693	chr7:102678544-102678545	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs138586272	chr7:102678569-102678570	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs141230691	chr7:102678601-102678602	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs530329355	chr7:102678604-102678605	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs563436438	chr7:102678640-102678641	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs548767764	chr7:102678652-102678653	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs569788707	chr7:102678653-102678654	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs116180541	chr7:102678668-102678669	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs552186784	chr7:102678672-102678673	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs570347275	chr7:102678675-102678676	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs534966377	chr7:102678676-102678677	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs115241217	chr7:102678692-102678693	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs183958896	chr7:102678708-102678709	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs535282090	chr7:102678717-102678718	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs548457000	chr7:102678729-102678730	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs556706907	chr7:102678730-102678731	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs374158860	chr7:102678733-102678734	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs576507413	chr7:102678738-102678739	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs543535378	chr7:102678749-102678750	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs369191808	chr7:102678770-102678771	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs150324995	chr7:102678781-102678782	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs541368209	chr7:102678782-102678783	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs560105532	chr7:102678800-102678801	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs554320973	chr7:102678823-102678824	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs371503096	chr7:102678859-102678860	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs548827984	chr7:102678867-102678868	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs369109676	chr7:102678894-102678895	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	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
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Autism	20531469	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102672000-102678400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:102676600-102683800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:102676800-102678000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr7:102677200-102679400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr7:102677400-102679800	Weak transcription	Right Atrium	heart
6	chr7:102677600-102679200	Flanking Active TSS	K562	blood
7	chr7:102677600-102679600	Enhancers	Stomach Mucosa	stomach
8	chr7:102678000-102678600	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr7:102678000-102678800	Enhancers	Gastric	stomach
10	chr7:102678200-102678400	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr7:102678200-102678400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr7:102678200-102678400	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr7:102678200-102678400	Enhancers	HepG2	liver
14	chr7:102678200-102678600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr7:102678200-102679200	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr7:102678400-102678600	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr7:102678400-102678600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr7:102678400-102678600	Enhancers	Pancreas	Pancrea
19	chr7:102678400-102678600	Flanking Active TSS	HepG2	liver
20	chr7:102678400-102678800	Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr7:102678400-102678800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr7:102678400-102678800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr7:102678400-102678800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
24	chr7:102678400-102678800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
25	chr7:102678400-102678800	Enhancers	Fetal Lung	lung
26	chr7:102678400-102679200	Enhancers	H9 Cell Line	embryonic stem cell
27	chr7:102678400-102679200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr7:102678400-102679200	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr7:102678400-102679200	Enhancers	Fetal Muscle Trunk	muscle
30	chr7:102678400-102679200	Enhancers	Lung	lung
31	chr7:102678600-102679000	Active TSS	HepG2	liver
32	chr7:102678600-102679200	Enhancers	Fetal Thymus	thymus
33	chr7:102678600-102684000	Weak transcription	Pancreas	Pancrea
34	chr7:102678600-102684600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr7:102678800-102679000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr7:102678800-102679400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr7:102678800-102679400	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr7:102679000-102679200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr7:102679000-102679200	Flanking Active TSS	HepG2	liver
40	chr7:102679200-102679400	Enhancers	K562	blood
41	chr7:102679200-102713800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr7:102679400-102679600	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr7:102682600-102688200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr7:102682800-102683600	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr7:102683400-102695800	Weak transcription	Fetal Kidney	kidney
46	chr7:102683600-102684200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
47	chr7:102683800-102684200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr7:102684000-102684200	ZNF genes & repeats	Pancreas	Pancrea
49	chr7:102684200-102690800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr7:102684200-102708000	Weak transcription	Pancreas	Pancrea

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