Variant report

Variant	nsv594582
Chromosome Location	chr4:69827340-69988378
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1357)
CpG islands
(count:427)
Chromatin interactive
region (count:8)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1357 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:69898611-69898899	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:69923214-69924064	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:69884842-69885191	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:69885882-69886539	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:69981638-69981898	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:69926532-69926534	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:69968302-69968701	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:69888831-69889086	HepG2	liver:	n/a	n/a
9	ARID3A	chr4:69890715-69891247	HepG2	liver:	n/a	n/a
10	ARID3A	chr4:69885444-69885630	HepG2	liver:	n/a	n/a
11	ARID3A	chr4:69920587-69920863	HepG2	liver:	n/a	n/a
12	ARID3A	chr4:69964127-69964803	HepG2	liver:	n/a	n/a
13	ARID3A	chr4:69960997-69962638	HepG2	liver:	n/a	n/a
14	ATF1	chr4:69932559-69932881	K562	blood:	n/a	n/a
15	ATF3	chr4:69961016-69961540	A549	lung:	n/a	n/a
16	ATF3	chr4:69961043-69961523	A549	lung:	n/a	n/a
17	ATF3	chr4:69900085-69900485	A549	lung:	n/a	n/a
18	BATF	chr4:69922672-69922971	GM12878	blood:	n/a	n/a
19	BATF	chr4:69904359-69904628	GM12878	blood:	n/a	chr4:69904462-69904472 chr4:69904458-69904468 chr4:69904461-69904472
20	BATF	chr4:69988219-69988511	GM12878	blood:	n/a	n/a
21	BATF	chr4:69988190-69988541	GM12878	blood:	n/a	n/a
22	BATF	chr4:69920558-69920852	GM12878	blood:	n/a	chr4:69920743-69920754
23	BATF	chr4:69920627-69920806	GM12878	blood:	n/a	chr4:69920743-69920754
24	BATF	chr4:69958781-69959019	GM12878	blood:	n/a	n/a
25	BATF	chr4:69917297-69917600	GM12878	blood:	n/a	n/a
26	BATF	chr4:69917171-69917689	GM12878	blood:	n/a	n/a
27	BCL11A	chr4:69917255-69917609	GM12878	blood:	n/a	n/a
28	BCL3	chr4:69960907-69962340	A549	lung:	n/a	n/a
29	BCL3	chr4:69885805-69886533	A549	lung:	n/a	n/a
30	BCL3	chr4:69961801-69962281	A549	lung:	n/a	n/a
31	BCL3	chr4:69900041-69900545	A549	lung:	n/a	n/a
32	BCL3	chr4:69899981-69900657	A549	lung:	n/a	n/a
33	BCL3	chr4:69898499-69898958	A549	lung:	n/a	n/a
34	BHLHE40	chr4:69959220-69959407	GM12878	blood:	n/a	n/a
35	BHLHE40	chr4:69917340-69917626	GM12878	blood:	n/a	n/a
36	BHLHE40	chr4:69921240-69921248	GM12878	blood:	n/a	n/a
37	BHLHE40	chr4:69932682-69932824	K562	blood:	n/a	n/a
38	BHLHE40	chr4:69920553-69920887	GM12878	blood:	n/a	n/a
39	BHLHE40	chr4:69852928-69852991	GM12878	blood:	n/a	n/a
40	BHLHE40	chr4:69984332-69984392	GM12878	blood:	n/a	n/a
41	BHLHE40	chr4:69924305-69924502	GM12878	blood:	n/a	n/a
42	BHLHE40	chr4:69923463-69923952	GM12878	blood:	n/a	n/a
43	CEBPB	chr4:69962103-69962398	HepG2	liver:	n/a	n/a
44	CEBPB	chr4:69886059-69886427	A549	lung:	n/a	n/a
45	CEBPB	chr4:69923273-69923624	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr4:69961795-69962072	HepG2	liver:	n/a	chr4:69961952-69961965 chr4:69961952-69961963 chr4:69961949-69961966 chr4:69961952-69961965
47	CEBPB	chr4:69886176-69886490	A549	lung:	n/a	n/a
48	CEBPB	chr4:69895793-69896419	HepG2	liver:	n/a	chr4:69896249-69896260 chr4:69896406-69896417 chr4:69896248-69896259 chr4:69896406-69896417
49	CEBPB	chr4:69968322-69968816	HepG2	liver:	n/a	n/a
50	CEBPB	chr4:69883582-69883882	HepG2	liver:	n/a	chr4:69883701-69883712 chr4:69883703-69883714 chr4:69883701-69883714 chr4:69883701-69883714

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69924245-69924295	BE2_C	brain:	n/a
2	chr4:69962676-69962726	T-47D	breast:	n/a
3	chr4:69962676-69962726	HL-60	blood:	n/a
4	chr4:69962676-69962726	SK-N-MC	brain:	n/a
5	chr4:69959004-69959054	K562	blood:	n/a
6	chr4:69976406-69976456	SK-N-SH_RA	brain:	n/a
7	chr4:69976406-69976456	Hela-S3	cervix:	n/a
8	chr4:69960869-69960919	Hepatocyte	liver:	n/a
9	chr4:69959004-69959054	HRCEpiC	kidney:	n/a
10	chr4:69959004-69959054	HNPCEpiC	eye:	n/a
11	chr4:69962676-69962726	GM12892	blood:	n/a
12	chr4:69960869-69960919	NB4	blood:	n/a
13	chr4:69859705-69859755	U87	brain:	n/a
14	chr4:69924245-69924295	SKMC	muscle:	n/a
15	chr4:69829409-69829459	AG09309	skin:	n/a
16	chr4:69829409-69829459	K562	blood:	n/a
17	chr4:69859705-69859755	HepG2	liver:	n/a
18	chr4:69976406-69976456	GM12892	blood:	n/a
19	chr4:69829409-69829459	PrEC	prostate:	n/a
20	chr4:69960869-69960919	BJ	skin:	n/a
21	chr4:69976406-69976456	SAEC	small airway:	n/a
22	chr4:69976406-69976456	HMEC	breast:	n/a
23	chr4:69976406-69976456	Caco-2	colon:	n/a
24	chr4:69859705-69859755	ProgFib	skin:	n/a
25	chr4:69959004-69959054	A549	lung:	n/a
26	chr4:69859705-69859755	GM19239	blood:	n/a
27	chr4:69962676-69962726	HRCEpiC	kidney:	n/a
28	chr4:69829409-69829459	HL-60	blood:	n/a
29	chr4:69962676-69962726	GM12891	blood:	n/a
30	chr4:69829409-69829459	HRE	kidney:	n/a
31	chr4:69829409-69829459	HRCEpiC	kidney:	n/a
32	chr4:69959004-69959054	HRE	kidney:	n/a
33	chr4:69859705-69859755	MCF10A-Er-Src	breast:	n/a
34	chr4:69829409-69829459	SK-N-SH	brain:	n/a
35	chr4:69976406-69976456	CMK	blood:	n/a
36	chr4:69959004-69959054	SK-N-MC	brain:	n/a
37	chr4:69924245-69924295	HRE	kidney:	n/a
38	chr4:69959004-69959054	Hepatocyte	liver:	n/a
39	chr4:69962676-69962726	HCPEpiC	choroid plexus:	n/a
40	chr4:69924245-69924295	HPAEpiC	pulmonary alveolar:	n/a
41	chr4:69924245-69924295	HUVEC	blood vessel:	n/a
42	chr4:69959004-69959054	HCT-116	colon:	n/a
43	chr4:69976406-69976456	U87	brain:	n/a
44	chr4:69859705-69859755	HEEpiC	esophagus:	n/a
45	chr4:69829409-69829459	GM19239	blood:	n/a
46	chr4:69959004-69959054	NHDF-neo	bronchial:	n/a
47	chr4:69859705-69859755	Hepatocyte	liver:	n/a
48	chr4:69959004-69959054	AG04450	lung:	fetal
49	chr4:69859705-69859755	HCF	heart:	n/a
50	chr4:69960869-69960919	HCT-116	colon:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:69981403..69984275-chr4:69989733..69991990,2	K562	blood:
2	chr4:69894916..69897017-chr4:69914362..69916605,2	MCF-7	breast:
3	chr4:69964055..69967936-chr4:69969110..69971498,3	K562	blood:
4	chr4:69894916..69897017-chr4:69914362..69916605,2	MCF-7	breast:
5	chr4:69925736..69927833-chr4:69929000..69931725,2	MCF-7	breast:
6	chr4:69964055..69967936-chr4:69969110..69971498,3	K562	blood:
7	chr4:69363348..69364328-chr4:69890914..69891634,2	MCF-7	breast:
8	chr4:69925736..69927833-chr4:69929000..69931725,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2A3-9	chr4:69887374-69888058	NONHSAT096750
2	lnc-UGT2A3-3	chr4:69840118-69840199	NONHSAT096748
3	lnc-UGT2A3-7	chr4:69862653-69863427	NONHSAT096749
4	lnc-UGT2A3-3	chr4:69838717-69838993	NONHSAT096748
5	lnc-UGT2A3-3	chr4:69839506-69839719	NONHSAT096748
6	lnc-UGT2B28-8	chr4:69935360-69935606	NONHSAT096752
7	lnc-UGT2A3-1	chr4:69914349-69914479	XLOC_003974
8	lnc-UGT2A3-3	chr4:69841579-69841711	NONHSAT096748
9	lnc-UGT2B28-8	chr4:69933121-69933337	NONHSAT096752
10	lnc-UGT2A3-1	chr4:69915661-69915748	XLOC_003974
11	lnc-UGT2B28-8	chr4:69932113-69932198	NONHSAT096752

No data

Variant related genes	Relation type
ENSG00000249890	TF binding region
ENSG00000249735	TF binding region
UGT2B7	TF binding region
ENSG00000248763	TF binding region
ENSG00000250919	TF binding region
ENSG00000251685	TF binding region
ENSG00000251284	TF binding region
ENSG00000251498	TF binding region
ENSG00000250277	TF binding region
ENSG00000249890	CpG island
ENSG00000249735	CpG island
UGT2B7	CpG island
ENSG00000248763	CpG island
ENSG00000250919	CpG island
ENSG00000251685	CpG island
ENSG00000251284	CpG island
ENSG00000251498	CpG island
ENSG00000250277	CpG island
ENSG00000251284	chromatin interactions
HERC4	miRNA target sites
MBNL3	miRNA target sites

Extended variants
information (count: 6990 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:6990 , 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	rs12513263	chr4:69827340-69827341	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs75998480	chr4:69827358-69827359	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189231942	chr4:69827363-69827364	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs34892848	chr4:69827364-69827365	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs116284083	chr4:69827414-69827415	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs181120531	chr4:69827430-69827431	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs72849640	chr4:69827455-69827456	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs570371017	chr4:69827471-69827472	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs28828979	chr4:69827491-69827492	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs141652703	chr4:69827500-69827501	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs117826653	chr4:69827501-69827502	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs111705024	chr4:69827502-69827503	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs111492960	chr4:69827523-69827524	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs186175218	chr4:69827536-69827537	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs111985681	chr4:69827550-69827551	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs190787683	chr4:69827564-69827565	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs150499450	chr4:69827565-69827566	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs577113190	chr4:69827596-69827597	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs546096826	chr4:69827600-69827601	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs35723612	chr4:69827601-69827602	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs559652511	chr4:69827624-69827625	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs528115934	chr4:69827659-69827660	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs111994485	chr4:69827661-69827662	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs139624562	chr4:69827668-69827669	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs12508920	chr4:69827688-69827689	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs12499093	chr4:69827705-69827706	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs564402671	chr4:69827727-69827728	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs570131139	chr4:69827757-69827758	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs183954483	chr4:69827809-69827810	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530826185	chr4:69827838-69827839	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs552464790	chr4:69827847-69827848	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs566002165	chr4:69827861-69827862	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs550376016	chr4:69827866-69827867	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs4487432	chr4:69827889-69827890	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs141924240	chr4:69828038-69828039	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs113759520	chr4:69828057-69828058	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs547977711	chr4:69828069-69828070	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs10033241	chr4:69828070-69828071	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs537145732	chr4:69828083-69828084	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs557147700	chr4:69828143-69828144	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs577095722	chr4:69828149-69828150	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs545993480	chr4:69828177-69828178	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs367843563	chr4:69828205-69828206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs533736242	chr4:69828237-69828238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs113143271	chr4:69828239-69828240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559690521	chr4:69828245-69828246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs146247854	chr4:69828257-69828258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs200280197	chr4:69828307-69828308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs541888681	chr4:69828308-69828309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs140169736	chr4:69828344-69828345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:634 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69820200-69828400	Weak transcription	Liver	Liver
2	chr4:69820400-69830000	Weak transcription	Small Intestine	intestine
3	chr4:69824600-69828200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr4:69825400-69827400	Enhancers	Rectal Mucosa Donor 29	rectum
5	chr4:69825800-69830200	Enhancers	Rectal Mucosa Donor 31	rectum
6	chr4:69826600-69830200	Enhancers	Fetal Intestine Large	intestine
7	chr4:69827000-69827800	Weak transcription	Pancreas	Pancrea
8	chr4:69827200-69827600	Weak transcription	HepG2	liver
9	chr4:69827200-69827800	Weak transcription	Fetal Intestine Small	intestine
10	chr4:69827400-69827600	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr4:69827600-69827800	Enhancers	HepG2	liver
12	chr4:69827600-69829800	Enhancers	Rectal Mucosa Donor 29	rectum
13	chr4:69827800-69828000	Enhancers	Pancreas	Pancrea
14	chr4:69827800-69829000	Weak transcription	HepG2	liver
15	chr4:69827800-69830600	Enhancers	Fetal Intestine Small	intestine
16	chr4:69828200-69828400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr4:69828400-69829000	Enhancers	Duodenum Mucosa	Duodenum
18	chr4:69828400-69829200	Enhancers	Fetal Heart	heart
19	chr4:69828400-69829400	Enhancers	Fetal Kidney	kidney
20	chr4:69828400-69829400	Enhancers	Stomach Mucosa	stomach
21	chr4:69828400-69829600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr4:69828400-69829800	Enhancers	Liver	Liver
23	chr4:69829000-69829400	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr4:69829000-69829400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr4:69829000-69829400	Enhancers	HepG2	liver
26	chr4:69829000-69829600	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr4:69829400-69835000	Weak transcription	Stomach Mucosa	stomach
28	chr4:69829600-69829800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:69829800-69830000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr4:69830000-69830400	Enhancers	Small Intestine	intestine
31	chr4:69830000-69833200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr4:69832600-69833000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr4:69833200-69842200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr4:69842200-69842600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr4:69842200-69842600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr4:69842400-69842800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr4:69842600-69846600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr4:69844800-69845200	Enhancers	Stomach Mucosa	stomach
39	chr4:69850200-69851600	Enhancers	Liver	Liver
40	chr4:69852800-69853400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr4:69853400-69856000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr4:69854200-69855200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr4:69854400-69855400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr4:69855200-69856000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
45	chr4:69858800-69860000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr4:69859800-69860200	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr4:69862000-69862200	Enhancers	Rectal Smooth Muscle	rectum
48	chr4:69862600-69863600	Weak transcription	Rectal Smooth Muscle	rectum
49	chr4:69862800-69863800	Enhancers	Fetal Stomach	stomach
50	chr4:69863600-69864200	Enhancers	Rectal Smooth Muscle	rectum

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