Variant report

Variant	nsv464266
Chromosome Location	chr7:3218524-3258801
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:589)
CpG islands
(count:551)
Chromatin interactive
region (count:26)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:589 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:3221006-3221355	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:3234233-3234865	HepG2	liver:	n/a	n/a
3	ATF2	chr7:3234272-3234806	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr7:3234177-3234810	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:3234182-3234735	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:3240149-3240409	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr7:3234202-3234797	A549	lung:	n/a	n/a
8	BCL3	chr7:3220998-3221446	GM12878	blood:	n/a	n/a
9	BCL3	chr7:3221093-3221491	GM12878	blood:	n/a	n/a
10	CEBPB	chr7:3234300-3234711	A549	lung:	n/a	n/a
11	CEBPB	chr7:3253725-3254035	HepG2	liver:	n/a	n/a
12	CEBPB	chr7:3234098-3234698	IMR90	lung:	n/a	n/a
13	CEBPB	chr7:3253684-3254018	A549	lung:	n/a	n/a
14	CEBPB	chr7:3253624-3254014	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr7:3255533-3256206	MCF-7	breast:	n/a	n/a
16	CEBPB	chr7:3255708-3255979	HepG2	liver:	n/a	n/a
17	CEBPB	chr7:3255447-3256238	MCF-7	breast:	n/a	n/a
18	CEBPB	chr7:3253683-3254028	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr7:3253634-3254152	A549	lung:	n/a	n/a
20	CEBPB	chr7:3234205-3234712	HepG2	liver:	n/a	n/a
21	CEBPB	chr7:3234293-3234711	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr7:3220965-3221379	HepG2	liver:	n/a	n/a
23	CEBPB	chr7:3253766-3254022	K562	blood:	n/a	n/a
24	CEBPB	chr7:3253762-3253885	HepG2	liver:	n/a	n/a
25	CEBPB	chr7:3221076-3221267	IMR90	lung:	n/a	n/a
26	CEBPB	chr7:3234322-3234665	A549	lung:	n/a	n/a
27	CEBPB	chr7:3258481-3258795	HepG2	liver:	n/a	chr7:3258619-3258630
28	CEBPB	chr7:3253649-3254023	A549	lung:	n/a	n/a
29	CEBPB	chr7:3253677-3254027	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr7:3253682-3253924	HepG2	liver:	n/a	n/a
31	CEBPB	chr7:3254435-3254556	A549	lung:	n/a	n/a
32	CEBPB	chr7:3234396-3234625	HepG2	liver:	n/a	n/a
33	CEBPB	chr7:3231891-3232043	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr7:3234374-3234541	K562	blood:	n/a	n/a
35	CEBPB	chr7:3253678-3254005	IMR90	lung:	n/a	n/a
36	CHD2	chr7:3221032-3221442	HepG2	liver:	n/a	n/a
37	CHD2	chr7:3234357-3234596	HepG2	liver:	n/a	n/a
38	CHD2	chr7:3243911-3244232	K562	blood:	n/a	n/a
39	CTBP2	chr7:3234305-3234912	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr7:3240220-3240370	GM12874	blood:	n/a	chr7:3240325-3240338 chr7:3240329-3240338 chr7:3240323-3240341
41	CTCF	chr7:3240260-3240410	HMEC	breast:	n/a	chr7:3240325-3240338 chr7:3240329-3240338 chr7:3240323-3240341
42	CTCF	chr7:3234300-3234450	GM12864	blood:	n/a	n/a
43	CTCF	chr7:3250254-3250377	HepG2	liver:	n/a	n/a
44	CTCF	chr7:3240052-3240575	MCF-7	breast:	n/a	chr7:3240325-3240338 chr7:3240329-3240338 chr7:3240323-3240341
45	CTCF	chr7:3240215-3240450	GM12878	blood:	n/a	chr7:3240325-3240338 chr7:3240329-3240338 chr7:3240323-3240341
46	CTCF	chr7:3234320-3234470	HAc	cerebellar:	n/a	n/a
47	CTCF	chr7:3240260-3240410	NHEK	skin:	n/a	chr7:3240325-3240338 chr7:3240329-3240338 chr7:3240323-3240341
48	CTCF	chr7:3234240-3234390	RPTEC	kidney:	n/a	n/a
49	CTCF	chr7:3239780-3239930	HVMF	connective:	n/a	n/a
50	CTCF	chr7:3240260-3240410	NB4	blood:	n/a	chr7:3240325-3240338 chr7:3240329-3240338 chr7:3240323-3240341

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:3221150-3221200	GM19239	blood:	n/a
2	chr7:3221150-3221200	RPTEC	kidney:	n/a
3	chr7:3221150-3221200	GM19239	blood:	n/a
4	chr7:3221150-3221200	RPTEC	kidney:	n/a
5	chr7:3227332-3227382	BJ	skin:	n/a
6	chr7:3221228-3221278	AG04449	skin:	fetal
7	chr7:3234697-3234747	ECC-1	luminal epithelium:	n/a
8	chr7:3221373-3221423	LNCaP	prostate:	n/a
9	chr7:3227332-3227382	GM06990	blood:	n/a
10	chr7:3227277-3227327	AG09309	skin:	n/a
11	chr7:3258347-3258397	GM12892	blood:	n/a
12	chr7:3227332-3227382	AG04450	lung:	fetal
13	chr7:3234697-3234747	PrEC	prostate:	n/a
14	chr7:3227332-3227382	HPAEpiC	pulmonary alveolar:	n/a
15	chr7:3227262-3227312	GM12891	blood:	n/a
16	chr7:3227277-3227327	SK-N-SH	brain:	n/a
17	chr7:3258347-3258397	HRPEpiC	eye:	n/a
18	chr7:3227277-3227327	K562	blood:	n/a
19	chr7:3221373-3221423	NT2-D1	testis:	n/a
20	chr7:3221150-3221200	GM12878	blood:	n/a
21	chr7:3256369-3256419	HEEpiC	esophagus:	n/a
22	chr7:3227277-3227327	HAEpiC	amniotic membrane:	n/a
23	chr7:3221150-3221200	Hela-S3	cervix:	n/a
24	chr7:3256369-3256419	ECC-1	luminal epithelium:	n/a
25	chr7:3258347-3258397	AoSMC	blood vessel:	n/a
26	chr7:3256369-3256419	T-47D	breast:	n/a
27	chr7:3234697-3234747	SK-N-SH	brain:	n/a
28	chr7:3221228-3221278	HepG2	liver:	n/a
29	chr7:3221373-3221423	GM12891	blood:	n/a
30	chr7:3258347-3258397	BE2_C	brain:	n/a
31	chr7:3227262-3227312	BJ	skin:	n/a
32	chr7:3234697-3234747	HEK293	kidney:	embryo
33	chr7:3221150-3221200	HUVEC	blood vessel:	n/a
34	chr7:3221150-3221200	HPAEpiC	pulmonary alveolar:	n/a
35	chr7:3227332-3227382	HCM	heart:	n/a
36	chr7:3258347-3258397	SAEC	small airway:	n/a
37	chr7:3227332-3227382	AG10803	skin:	n/a
38	chr7:3227332-3227382	GM12891	blood:	n/a
39	chr7:3221228-3221278	LNCaP	prostate:	n/a
40	chr7:3234697-3234747	LNCaP	prostate:	n/a
41	chr7:3221373-3221423	NH-A	brain:	n/a
42	chr7:3221228-3221278	H1-hESC	embryonic stem cell:	embryo
43	chr7:3227277-3227327	HCPEpiC	choroid plexus:	n/a
44	chr7:3221228-3221278	GM19239	blood:	n/a
45	chr7:3221228-3221278	PFSK-1	brain:	n/a
46	chr7:3221373-3221423	NHBE	bronchial:	n/a
47	chr7:3234697-3234747	AG09309	skin:	n/a
48	chr7:3227262-3227312	HPAEpiC	pulmonary alveolar:	n/a
49	chr7:3221373-3221423	SKMC	muscle:	n/a
50	chr7:3227332-3227382	K562	blood:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:2926249..2926927-chr7:3240062..3240775,2	MCF-7	breast:
2	chr7:3254337..3257238-chr7:3340637..3342323,2	MCF-7	breast:
3	chr7:3251471..3253553-chr7:3281258..3284246,2	MCF-7	breast:
4	chr7:3255932..3258041-chr7:3261586..3263750,2	MCF-7	breast:
5	chr7:3227729..3230209-chr7:3232264..3234725,2	MCF-7	breast:
6	chr7:3128837..3129871-chr7:3239803..3240577,4	MCF-7	breast:
7	chr7:3201417..3202351-chr7:3240242..3240878,3	MCF-7	breast:
8	chr7:3254572..3259584-chr7:3282203..3284323,4	MCF-7	breast:
9	chr7:3256947..3259532-chr7:3270807..3273199,2	MCF-7	breast:
10	chr7:3205607..3207977-chr7:3220687..3223407,2	K562	blood:
11	chr7:3104998..3105685-chr7:3239854..3240733,2	MCF-7	breast:
12	chr7:3255775..3258559-chr7:3276222..3279313,3	MCF-7	breast:
13	chr7:3254030..3256348-chr7:3338235..3340171,2	MCF-7	breast:
14	chr7:2915975..2917721-chr7:3231286..3232804,2	MCF-7	breast:
15	chr7:3210592..3212478-chr7:3220599..3222530,2	K562	blood:
16	chr7:3255245..3256305-chr7:3283809..3284534,3	MCF-7	breast:
17	chr7:2912750..2915143-chr7:3228683..3231010,3	MCF-7	breast:
18	chr7:3253620..3255788-chr7:3339992..3342861,2	MCF-7	breast:
19	chr7:2926533..2927268-chr7:3239915..3240463,3	MCF-7	breast:
20	chr7:3250247..3250807-chr7:3340190..3341077,3	MCF-7	breast:
21	chr7:3255528..3257837-chr7:3259945..3262892,2	MCF-7	breast:
22	chr7:3249846..3250536-chr7:3341685..3342449,3	MCF-7	breast:
23	chr7:2921568..2923869-chr7:3228214..3231115,2	MCF-7	breast:
24	chr7:3227729..3230209-chr7:3232264..3234725,2	MCF-7	breast:
25	chr7:3254376..3256017-chr7:3281440..3283827,2	MCF-7	breast:
26	chr7:3240198..3242825-chr7:3445733..3447901,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC091801.1.1-4	chr7:3242576-3242787	XLOC_006342
2	lnc-AC091801.1.1-2	chr7:3233737-3234256	XLOC_006340
3	lnc-AC091801.1.1-2	chr7:3234354-3234428	XLOC_006340
4	lnc-AC091801.1.1-4	chr7:3243575-3243666	XLOC_006342

No data

Variant related genes	Relation type
ENSG00000217455	TF binding region
ENSG00000231892	TF binding region
ENSG00000217455	CpG island
ENSG00000231892	CpG island
ENSG00000236708	chromatin interactions
ENSG00000146555	chromatin interactions
HIPK3	miRNA target sites

Extended variants
information (count: 2345 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:2345 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7785633	chr7:3218524-3218525	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs185266809	chr7:3218581-3218582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs556043096	chr7:3218596-3218597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs375130395	chr7:3218602-3218603	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs148118255	chr7:3218605-3218606	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs560275578	chr7:3218606-3218607	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs141878446	chr7:3218610-3218611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs35763360	chr7:3218616-3218617	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs75967380	chr7:3218619-3218620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs150616630	chr7:3218650-3218651	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559619667	chr7:3218663-3218664	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs118140685	chr7:3218673-3218674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550571481	chr7:3218676-3218677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570774553	chr7:3218699-3218700	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs533699183	chr7:3218734-3218735	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547006307	chr7:3218767-3218768	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs369467282	chr7:3218776-3218777	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551395075	chr7:3218799-3218800	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs535710812	chr7:3218813-3218814	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs567026323	chr7:3218814-3218815	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs112272493	chr7:3218821-3218822	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs568975522	chr7:3218830-3218831	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs537799418	chr7:3218838-3218839	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs557810107	chr7:3218843-3218844	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs574270200	chr7:3218891-3218892	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs139672316	chr7:3218892-3218893	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs34331963	chr7:3218900-3218901	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs377439016	chr7:3218936-3218937	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs573780215	chr7:3218962-3218963	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs542418526	chr7:3218966-3218967	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs561808956	chr7:3218980-3218981	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs17799341	chr7:3218987-3218988	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs544170518	chr7:3219023-3219024	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs59436545	chr7:3219029-3219030	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs142990124	chr7:3219056-3219057	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs553157143	chr7:3219142-3219143	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs547260087	chr7:3219153-3219154	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs17133109	chr7:3219163-3219164	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs529441060	chr7:3219177-3219178	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs147548404	chr7:3219182-3219183	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs568936356	chr7:3219203-3219204	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs188534185	chr7:3219204-3219205	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs140169234	chr7:3219254-3219255	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs538548586	chr7:3219273-3219274	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs191636905	chr7:3219275-3219276	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs374161517	chr7:3219295-3219296	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs145592419	chr7:3219322-3219323	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs553990193	chr7:3219323-3219324	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs145311480	chr7:3219356-3219357	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs184181794	chr7:3219374-3219375	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
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
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Nasopharyngeal cancer	20548289	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:327 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3205200-3221000	Weak transcription	Right Atrium	heart
2	chr7:3215600-3219000	Weak transcription	Fetal Brain Male	brain
3	chr7:3215800-3220200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr7:3216400-3218800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr7:3216400-3219800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr7:3216600-3220400	Weak transcription	Pancreas	Pancrea
7	chr7:3216800-3218600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr7:3216800-3232600	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr7:3218400-3218800	Enhancers	HepG2	liver
10	chr7:3218600-3219400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr7:3218800-3219000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr7:3218800-3219600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr7:3218800-3219600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr7:3218800-3219800	Flanking Active TSS	HepG2	liver
15	chr7:3219000-3219200	Enhancers	Fetal Brain Male	brain
16	chr7:3219200-3220200	Weak transcription	Fetal Brain Male	brain
17	chr7:3219600-3223800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr7:3219800-3220400	Enhancers	HepG2	liver
19	chr7:3220200-3220600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr7:3220200-3222800	Enhancers	Fetal Brain Male	brain
21	chr7:3220400-3220600	Enhancers	Pancreas	Pancrea
22	chr7:3220400-3220600	Flanking Active TSS	HepG2	liver
23	chr7:3220400-3221600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr7:3220600-3221000	Weak transcription	Pancreas	Pancrea
25	chr7:3220600-3221000	Enhancers	HepG2	liver
26	chr7:3220600-3228600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr7:3221000-3221200	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
28	chr7:3221000-3221200	Bivalent Enhancer	Fetal Muscle Leg	muscle
29	chr7:3221000-3221200	Enhancers	Rectal Smooth Muscle	rectum
30	chr7:3221000-3221200	Flanking Active TSS	Right Atrium	heart
31	chr7:3221000-3221200	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
32	chr7:3221000-3221400	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr7:3221000-3221400	Active TSS	Colon Smooth Muscle	Colon
34	chr7:3221000-3221400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
35	chr7:3221000-3221400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr7:3221000-3221400	Enhancers	Ovary	ovary
37	chr7:3221000-3221400	Enhancers	Pancreas	Pancrea
38	chr7:3221000-3221400	Flanking Active TSS	HepG2	liver
39	chr7:3221000-3221600	Flanking Bivalent TSS/Enh	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr7:3221000-3221600	Active TSS	Right Ventricle	heart
41	chr7:3221000-3221600	Enhancers	NHEK	skin
42	chr7:3221000-3222800	Enhancers	Fetal Stomach	stomach
43	chr7:3221200-3221400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr7:3221200-3221400	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
45	chr7:3221200-3221400	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
46	chr7:3221200-3221400	Active TSS	Fetal Brain Female	brain
47	chr7:3221200-3221400	Enhancers	Fetal Lung	lung
48	chr7:3221200-3221400	Enhancers	Gastric	stomach
49	chr7:3221200-3221400	Active TSS	Right Atrium	heart
50	chr7:3221200-3221400	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach

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