Variant report

Variant	nsv948605
Chromosome Location	chr7:80119690-80298887
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1700)
CpG islands
(count:1100)
Chromatin interactive
region (count:24)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1700 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:80128367-80129128	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:80144844-80144963	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:80240786-80241747	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:80263770-80264169	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:80284287-80284555	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:80288875-80289153	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:80218074-80218152	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:80272116-80272564	HepG2	liver:	n/a	n/a
9	ATF2	chr7:80267373-80268134	GM12878	blood:	n/a	n/a
10	ATF2	chr7:80267578-80268064	GM12878	blood:	n/a	n/a
11	BACH1	chr7:80260910-80260913	K562	blood:	n/a	n/a
12	BACH1	chr7:80217948-80218267	H1-hESC	embryonic stem cell:	n/a	chr7:80218106-80218120
13	BACH1	chr7:80128743-80128980	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr7:80267647-80267923	GM12878	blood:	n/a	n/a
15	BATF	chr7:80221037-80221261	GM12878	blood:	n/a	n/a
16	BATF	chr7:80267605-80267988	GM12878	blood:	n/a	n/a
17	BCL11A	chr7:80267588-80268026	GM12878	blood:	n/a	n/a
18	BCL11A	chr7:80267684-80267984	GM12878	blood:	n/a	n/a
19	BCL3	chr7:80267478-80268093	GM12878	blood:	n/a	chr7:80267573-80267582
20	BCL3	chr7:80241066-80241560	A549	lung:	n/a	n/a
21	BCL3	chr7:80127785-80128117	GM12878	blood:	n/a	n/a
22	BCLAF1	chr7:80267523-80268057	GM12878	blood:	n/a	chr7:80267573-80267582
23	BHLHE40	chr7:80267457-80267965	GM12878	blood:	n/a	n/a
24	BHLHE40	chr7:80241129-80241645	HepG2	liver:	n/a	n/a
25	BRCA1	chr7:80288768-80289107	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr7:80263685-80264171	Hela-S3	cervix:	n/a	n/a
27	CCNT2	chr7:80127711-80127911	K562	blood:	n/a	n/a
28	CEBPB	chr7:80181336-80181974	Hela-S3	cervix:	n/a	chr7:80181824-80181835 chr7:80181822-80181834 chr7:80181815-80181826
29	CEBPB	chr7:80128302-80128946	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr7:80171655-80172186	Hela-S3	cervix:	n/a	chr7:80171841-80171858 chr7:80171742-80171753
31	CEBPB	chr7:80179406-80179609	Hela-S3	cervix:	n/a	chr7:80179510-80179521 chr7:80179508-80179519
32	CEBPB	chr7:80179385-80179612	IMR90	lung:	n/a	chr7:80179510-80179521 chr7:80179508-80179519
33	CEBPB	chr7:80214088-80214466	A549	lung:	n/a	chr7:80214295-80214312 chr7:80214191-80214202
34	CEBPB	chr7:80171764-80172123	A549	lung:	n/a	chr7:80171841-80171858
35	CEBPB	chr7:80214073-80214485	Hela-S3	cervix:	n/a	chr7:80214295-80214312 chr7:80214191-80214202
36	CEBPB	chr7:80262315-80262400	A549	lung:	n/a	chr7:80262334-80262345
37	CEBPB	chr7:80263757-80264252	A549	lung:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
38	CEBPB	chr7:80223156-80223784	A549	lung:	n/a	chr7:80223612-80223623
39	CEBPB	chr7:80169797-80170029	H1-hESC	embryonic stem cell:	n/a	chr7:80169926-80169939 chr7:80169928-80169939 chr7:80169926-80169937
40	CEBPB	chr7:80210873-80211099	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr7:80144819-80145031	HepG2	liver:	n/a	chr7:80144903-80144914
42	CEBPB	chr7:80263870-80264032	K562	blood:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
43	CEBPB	chr7:80263755-80264281	Hela-S3	cervix:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
44	CEBPB	chr7:80252795-80253074	HepG2	liver:	n/a	chr7:80252895-80252908 chr7:80252895-80252906 chr7:80252913-80252926 chr7:80252897-80252908 chr7:80252915-80252926 chr7:80252895-80252908 chr7:80252915-80252926 chr7:80252913-80252926 chr7:80252913-80252924 chr7:80252895-80252908
45	CEBPB	chr7:80272148-80272537	HepG2	liver:	n/a	chr7:80272335-80272348 chr7:80272335-80272346
46	CEBPB	chr7:80241130-80241436	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr7:80128357-80128974	MCF-7	breast:	n/a	n/a
48	CEBPB	chr7:80263777-80264203	HepG2	liver:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
49	CEBPB	chr7:80179379-80179672	K562	blood:	n/a	chr7:80179510-80179521 chr7:80179508-80179519
50	CEBPB	chr7:80135250-80135976	MCF-7	breast:	n/a	chr7:80135843-80135854

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:80230544-80230594	T-47D	breast:	n/a
2	chr7:80142060-80142110	Hela-S3	cervix:	n/a
3	chr7:80230544-80230594	T-47D	breast:	n/a
4	chr7:80142060-80142110	Hela-S3	cervix:	n/a
5	chr7:80291794-80291844	Hela-S3	cervix:	n/a
6	chr7:80236112-80236162	MCF10A-Er-Src	breast:	n/a
7	chr7:80230525-80230575	Hepatocyte	liver:	n/a
8	chr7:80252533-80252583	LNCaP	prostate:	n/a
9	chr7:80267619-80267669	HUVEC	blood vessel:	n/a
10	chr7:80275870-80275920	GM12892	blood:	n/a
11	chr7:80142060-80142110	SK-N-SH_RA	brain:	n/a
12	chr7:80274460-80274510	NHBE	bronchial:	n/a
13	chr7:80267619-80267669	HEEpiC	esophagus:	n/a
14	chr7:80231599-80231649	NHDF-neo	bronchial:	n/a
15	chr7:80142634-80142684	NHDF-neo	bronchial:	n/a
16	chr7:80275870-80275920	PFSK-1	brain:	n/a
17	chr7:80267619-80267669	AoSMC	blood vessel:	n/a
18	chr7:80230528-80230578	AG04450	lung:	fetal
19	chr7:80230528-80230578	NB4	blood:	n/a
20	chr7:80230528-80230578	ovcar-3	ovarian:	n/a
21	chr7:80142060-80142110	AG04450	lung:	fetal
22	chr7:80142634-80142684	SK-N-MC	brain:	n/a
23	chr7:80267619-80267669	SKMC	muscle:	n/a
24	chr7:80266930-80266980	GM12878	blood:	n/a
25	chr7:80236112-80236162	HCPEpiC	choroid plexus:	n/a
26	chr7:80267943-80267993	AG04450	lung:	fetal
27	chr7:80230525-80230575	HAEpiC	amniotic membrane:	n/a
28	chr7:80230525-80230575	NH-A	brain:	n/a
29	chr7:80275870-80275920	SK-N-SH	brain:	n/a
30	chr7:80267943-80267993	HIPEpiC	eye:	n/a
31	chr7:80291794-80291844	BJ	skin:	n/a
32	chr7:80230528-80230578	HL-60	blood:	n/a
33	chr7:80236112-80236162	NB4	blood:	n/a
34	chr7:80244500-80244550	AG10803	skin:	n/a
35	chr7:80230062-80230112	ovcar-3	ovarian:	n/a
36	chr7:80230544-80230594	GM12891	blood:	n/a
37	chr7:80236112-80236162	HNPCEpiC	eye:	n/a
38	chr7:80291794-80291844	PFSK-1	brain:	n/a
39	chr7:80267619-80267669	AG09319	gingival:	n/a
40	chr7:80291832-80291882	HEK293	kidney:	embryo
41	chr7:80275870-80275920	Jurkat	blood:	n/a
42	chr7:80274460-80274510	PFSK-1	brain:	n/a
43	chr7:80252533-80252583	HL-60	blood:	n/a
44	chr7:80266930-80266980	AG10803	skin:	n/a
45	chr7:80267619-80267669	Hela-S3	cervix:	n/a
46	chr7:80142060-80142110	SK-N-MC	brain:	n/a
47	chr7:80244500-80244550	BJ	skin:	n/a
48	chr7:80275870-80275920	BE2_C	brain:	n/a
49	chr7:80275870-80275920	Hepatocyte	liver:	n/a
50	chr7:80230062-80230112	HAEpiC	amniotic membrane:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:80290704..80291673-chr7:80310324..80310826,2	MCF-7	breast:
2	chr7:80239752..80242160-chr7:80242540..80244695,3	K562	blood:
3	chr7:80296853..80299195-chr7:80307235..80310003,2	MCF-7	breast:
4	chr7:80057613..80058392-chr7:80288390..80289288,3	MCF-7	breast:
5	chr7:80130973..80133838-chr7:80134281..80135849,2	MCF-7	breast:
6	chr7:80215015..80216821-chr7:80218593..80220289,2	K562	blood:
7	chr7:80125854..80128249-chr7:80143744..80146199,2	MCF-7	breast:
8	chr7:80239752..80242160-chr7:80242540..80244695,3	K562	blood:
9	chr7:80198036..80200312-chr7:80208194..80210191,2	MCF-7	breast:
10	chr7:80179936..80183033-chr7:80192105..80194774,3	MCF-7	breast:
11	chr7:80057471..80058066-chr7:80288234..80289022,3	MCF-7	breast:
12	chr7:80130973..80133838-chr7:80134281..80135849,2	MCF-7	breast:
13	chr7:80179936..80183033-chr7:80192105..80194774,3	MCF-7	breast:
14	chr7:80215015..80216821-chr7:80218593..80220289,2	K562	blood:
15	chr7:80254055..80256546-chr7:80258500..80261458,2	K562	blood:
16	chr7:80230076..80232841-chr7:80236237..80238542,2	MCF-7	breast:
17	chr7:80288156..80289657-chr7:80291382..80293831,2	K562	blood:
18	chr7:80125854..80128249-chr7:80143744..80146199,2	MCF-7	breast:
19	chr7:80057560..80058347-chr7:80243745..80244716,2	MCF-7	breast:
20	chr7:80139898..80142086-chr7:80143666..80145731,2	MCF-7	breast:
21	chr7:80291053..80291665-chr7:81099051..81099939,2	MCF-7	breast:
22	chr7:80198036..80200312-chr7:80208194..80210191,2	MCF-7	breast:
23	chr7:80263049..80265695-chr7:80267263..80270319,3	K562	blood:
24	chr7:80226468..80229283-chr7:80231335..80233921,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GNAI1-5	chr7:80275968-80276042	NONHSAT121746
2	lnc-GNAI1-5	chr7:80275404-80275497	NONHSAT121746
3	lnc-GNAI1-5	chr7:80231466-80231695	NONHSAT121745
4	lnc-GNAI1-4	chr7:80253211-80253506	NONHSAT121747
5	lnc-GNAI1-4	chr7:80262513-80262678	NONHSAT121747
6	lnc-GNAI1-5	chr7:80266148-80266319	NONHSAT121746
7	lnc-GNAI1-5	chr7:80275404-80275497	NONHSAT121745
8	lnc-GNAI1-5	chr7:80231541-80231695	NONHSAT121746
9	lnc-GNAI1-5	chr7:80275968-80276531	NONHSAT121745

No data

Variant related genes	Relation type
CD36	TF binding region
ENSG00000229436	TF binding region
GNAT3	TF binding region
CD36	CpG island
ENSG00000229436	CpG island
GNAT3	CpG island
ENSG00000214415	chromatin interactions
ENSG00000229436	chromatin interactions
ENSG00000135218	chromatin interactions

Extended variants
information (count: 6960 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:6960 , 50 per page) page: 1 2 3 4 5 6 7 ... 140

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11978272	chr7:80119690-80119691	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs148642960	chr7:80119700-80119701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs10242727	chr7:80119730-80119731	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs372486217	chr7:80119758-80119759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs76178572	chr7:80119835-80119836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs113092666	chr7:80119858-80119859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs113908042	chr7:80119867-80119868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs557702767	chr7:80119886-80119887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs578004632	chr7:80119896-80119897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs141183146	chr7:80119927-80119928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540160398	chr7:80119972-80119973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552916975	chr7:80119989-80119990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572912371	chr7:80119991-80119992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs11972427	chr7:80119997-80119998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs541875801	chr7:80120071-80120072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs150720244	chr7:80120094-80120095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs139065269	chr7:80120100-80120101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs541488621	chr7:80120108-80120109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs111467128	chr7:80120112-80120113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs186453030	chr7:80120118-80120119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs190814981	chr7:80120233-80120234	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547331541	chr7:80120274-80120275	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs566434421	chr7:80120302-80120303	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs143984786	chr7:80120320-80120321	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs548744910	chr7:80120368-80120369	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568919065	chr7:80120399-80120400	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540279900	chr7:80120418-80120419	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs551526021	chr7:80120423-80120424	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560604086	chr7:80120429-80120430	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533797354	chr7:80120432-80120433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553657098	chr7:80120438-80120439	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs573647211	chr7:80120447-80120448	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535829588	chr7:80120542-80120543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146040697	chr7:80120543-80120544	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs139960586	chr7:80120561-80120562	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs544399735	chr7:80120573-80120574	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564667110	chr7:80120608-80120609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs578223197	chr7:80120700-80120701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs540881800	chr7:80120720-80120721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs73369046	chr7:80120729-80120730	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs143399620	chr7:80120775-80120776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs549178986	chr7:80120814-80120815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs548942931	chr7:80120861-80120862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs559391268	chr7:80120867-80120868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs113606512	chr7:80120878-80120879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs182715676	chr7:80120895-80120896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs531403361	chr7:80120954-80120955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs562708065	chr7:80121021-80121022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs551198410	chr7:80121028-80121029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs373361556	chr7:80121037-80121038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Neurodevelopmental disorder	22521361	CNVD
Williams Syndrome	20824207	CNVD
Metanephric adenoma	20802469	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Williams-beuren syndrome	16826523	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	19318497	CNVD
Multiple myeloma	16616336	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
Cancer	20164919	CNVD
Breast cancer	21611746	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:1629 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:80113000-80127800	Weak transcription	Hela-S3	cervix
2	chr7:80118600-80120600	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr7:80118600-80122800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr7:80118600-80127400	Weak transcription	NHEK	skin
5	chr7:80118800-80120200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr7:80118800-80120600	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr7:80118800-80121000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr7:80119000-80120800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr7:80119000-80122400	Weak transcription	NHDF-Ad	bronchial
10	chr7:80119400-80120400	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr7:80120200-80120600	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr7:80120400-80121400	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr7:80120600-80120800	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr7:80120600-80121000	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr7:80120600-80121400	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr7:80120600-80128000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr7:80120800-80121200	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr7:80121000-80121200	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr7:80121200-80125200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr7:80121400-80128400	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr7:80121400-80128400	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr7:80122400-80123000	Enhancers	NHDF-Ad	bronchial
23	chr7:80122800-80123200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
24	chr7:80123000-80127400	Weak transcription	NHDF-Ad	bronchial
25	chr7:80125200-80125400	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr7:80125200-80125600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr7:80125400-80125600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr7:80125600-80127400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr7:80125600-80128400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr7:80125800-80128200	Enhancers	Muscle Satellite Cultured Cells	--
31	chr7:80126000-80126200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr7:80126000-80126200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr7:80126000-80126200	Enhancers	A549	lung
34	chr7:80126000-80129800	Enhancers	Osteobl	bone
35	chr7:80126000-80130600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr7:80126200-80127400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr7:80126200-80127400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr7:80126200-80130000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr7:80126200-80130000	Enhancers	NHLF	lung
40	chr7:80126200-80130400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr7:80126400-80126600	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr7:80126400-80126600	Enhancers	NH-A	brain
43	chr7:80126400-80127600	Weak transcription	A549	lung
44	chr7:80126400-80128200	Enhancers	HSMMtube	muscle
45	chr7:80126600-80126800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr7:80126600-80126800	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr7:80126600-80127200	Weak transcription	NH-A	brain
48	chr7:80126600-80127400	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr7:80126600-80129600	Enhancers	HSMM	muscle
50	chr7:80126800-80127400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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