Variant report

Variant	esv2760851
Chromosome Location	chr4:77164549-77185144
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:516)
CpG islands
(count:857)
Chromatin interactive
region (count:19)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:516 , 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	chr4:77177420-77177437	K562	blood:	n/a	n/a
2	ARID3A	chr4:77172714-77173123	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:77178234-77178371	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:77181797-77182144	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:77170711-77170737	K562	blood:	n/a	n/a
6	BACH1	chr4:77172689-77173191	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:77177393-77177463	K562	blood:	n/a	n/a
8	BACH1	chr4:77174376-77174464	K562	blood:	n/a	n/a
9	BHLHE40	chr4:77172282-77172391	K562	blood:	n/a	n/a
10	BHLHE40	chr4:77172572-77173142	HepG2	liver:	n/a	n/a
11	BHLHE40	chr4:77177255-77177603	K562	blood:	n/a	n/a
12	BHLHE40	chr4:77179150-77179357	HepG2	liver:	n/a	n/a
13	CCNT2	chr4:77172724-77173129	K562	blood:	n/a	n/a
14	CCNT2	chr4:77177366-77177961	K562	blood:	n/a	n/a
15	CEBPB	chr4:77168021-77168311	K562	blood:	n/a	chr4:77168196-77168207 chr4:77168177-77168188
16	CEBPB	chr4:77168136-77168330	A549	lung:	n/a	chr4:77168196-77168207 chr4:77168177-77168188
17	CEBPB	chr4:77182836-77182974	IMR90	lung:	n/a	chr4:77182920-77182931
18	CEBPB	chr4:77183304-77183581	HepG2	liver:	n/a	chr4:77183432-77183443
19	CEBPB	chr4:77182781-77183030	HepG2	liver:	n/a	chr4:77182920-77182931
20	CEBPB	chr4:77184326-77184504	A549	lung:	n/a	n/a
21	CEBPB	chr4:77177285-77177485	K562	blood:	n/a	n/a
22	CEBPB	chr4:77168070-77168289	HepG2	liver:	n/a	chr4:77168196-77168207 chr4:77168177-77168188
23	CEBPB	chr4:77172614-77173052	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr4:77183344-77183611	K562	blood:	n/a	chr4:77183432-77183443
25	CEBPD	chr4:77172787-77173062	HepG2	liver:	n/a	n/a
26	CHD2	chr4:77172755-77173031	HepG2	liver:	n/a	n/a
27	CHD2	chr4:77177362-77177367	K562	blood:	n/a	n/a
28	CHD2	chr4:77172619-77172963	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr4:77172627-77173056	A549	lung:	n/a	n/a
30	CTCF	chr4:77179080-77179230	SAEC	small airway:	n/a	chr4:77179175-77179193 chr4:77179177-77179190
31	CTCF	chr4:77172846-77173182	MCF-7	breast:	n/a	n/a
32	CTCF	chr4:77172927-77173094	LNCaP	prostate:	n/a	n/a
33	CTCF	chr4:77167320-77167470	HMEC	breast:	n/a	n/a
34	CTCF	chr4:77172916-77173120	GM12892	blood:	n/a	n/a
35	CTCF	chr4:77172880-77173030	BJ	skin:	n/a	n/a
36	CTCF	chr4:77172926-77173125	K562	blood:	n/a	n/a
37	CTCF	chr4:77172850-77173183	K562	blood:	n/a	n/a
38	CTCF	chr4:77172940-77173090	HVMF	connective:	n/a	n/a
39	CTCF	chr4:77167261-77167495	MCF-7	breast:	n/a	n/a
40	CTCF	chr4:77172941-77173109	GM10248	blood:	n/a	n/a
41	CTCF	chr4:77172920-77173070	GM12867	blood:	n/a	n/a
42	CTCF	chr4:77172891-77173098	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr4:77172983-77173085	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr4:77172850-77173162	MCF-7	breast:	n/a	n/a
45	CTCF	chr4:77179120-77179270	SAEC	small airway:	n/a	chr4:77179175-77179193 chr4:77179177-77179190
46	CTCF	chr4:77167340-77167490	HEEpiC	esophagus:	n/a	n/a
47	CTCF	chr4:77172900-77173050	HRE	kidney:	n/a	n/a
48	CTCF	chr4:77172980-77173130	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr4:77172875-77173173	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr4:77172940-77173090	GM12869	blood:	n/a	n/a

(count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:77173119-77173169	Caco-2	colon:	n/a
2	chr4:77170672-77170722	PrEC	prostate:	n/a
3	chr4:77173197-77173247	Jurkat	blood:	n/a
4	chr4:77173119-77173169	Caco-2	colon:	n/a
5	chr4:77170672-77170722	PrEC	prostate:	n/a
6	chr4:77173197-77173247	Jurkat	blood:	n/a
7	chr4:77176869-77176919	AoSMC	blood vessel:	n/a
8	chr4:77172861-77172911	GM06990	blood:	n/a
9	chr4:77173197-77173247	GM12892	blood:	n/a
10	chr4:77172841-77172891	GM12892	blood:	n/a
11	chr4:77173119-77173169	HCPEpiC	choroid plexus:	n/a
12	chr4:77184168-77184218	GM12878	blood:	n/a
13	chr4:77172617-77172667	SKMC	muscle:	n/a
14	chr4:77172699-77172749	CMK	blood:	n/a
15	chr4:77170672-77170722	MCF10A-Er-Src	breast:	n/a
16	chr4:77172836-77172886	HMEC	breast:	n/a
17	chr4:77172861-77172911	GM19239	blood:	n/a
18	chr4:77172836-77172886	AG09309	skin:	n/a
19	chr4:77172699-77172749	K562	blood:	n/a
20	chr4:77172699-77172749	SKMC	muscle:	n/a
21	chr4:77172861-77172911	K562	blood:	n/a
22	chr4:77172841-77172891	NH-A	brain:	n/a
23	chr4:77172660-77172710	GM19239	blood:	n/a
24	chr4:77172861-77172911	GM12878	blood:	n/a
25	chr4:77172841-77172891	HEK293	kidney:	embryo
26	chr4:77168991-77169041	HL-60	blood:	n/a
27	chr4:77170672-77170722	SK-N-MC	brain:	n/a
28	chr4:77170672-77170722	SAEC	small airway:	n/a
29	chr4:77170672-77170722	HRE	kidney:	n/a
30	chr4:77184168-77184218	BJ	skin:	n/a
31	chr4:77173001-77173051	U87	brain:	n/a
32	chr4:77170672-77170722	NH-A	brain:	n/a
33	chr4:77172841-77172891	SK-N-SH_RA	brain:	n/a
34	chr4:77184168-77184218	BE2_C	brain:	n/a
35	chr4:77173119-77173169	T-47D	breast:	n/a
36	chr4:77173197-77173247	Hela-S3	cervix:	n/a
37	chr4:77172660-77172710	SK-N-SH	brain:	n/a
38	chr4:77172841-77172891	ovcar-3	ovarian:	n/a
39	chr4:77173001-77173051	SK-N-SH	brain:	n/a
40	chr4:77172841-77172891	HCT-116	colon:	n/a
41	chr4:77172660-77172710	HRCEpiC	kidney:	n/a
42	chr4:77172861-77172911	H1-hESC	embryonic stem cell:	embryo
43	chr4:77173197-77173247	HCF	heart:	n/a
44	chr4:77173119-77173169	H1-hESC	embryonic stem cell:	embryo
45	chr4:77172643-77172693	NH-A	brain:	n/a
46	chr4:77173197-77173247	AG10803	skin:	n/a
47	chr4:77172861-77172911	NB4	blood:	n/a
48	chr4:77170672-77170722	NHDF-neo	bronchial:	n/a
49	chr4:77172836-77172886	ovcar-3	ovarian:	n/a
50	chr4:77172617-77172667	NHBE	bronchial:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:77157429..77161851-chr4:77161856..77166558,5	MCF-7	breast:
2	chr4:77133278..77135557-chr4:77171656..77174471,3	MCF-7	breast:
3	chr4:77165064..77167493-chr4:77174521..77177235,2	K562	blood:
4	chr4:77155513..77160129-chr4:77161084..77164552,4	MCF-7	breast:
5	chr4:77171208..77175531-chr4:77176138..77180024,6	K562	blood:
6	chr4:77161340..77163165-chr4:77170390..77172586,2	MCF-7	breast:
7	chr4:77171208..77175531-chr4:77176138..77180024,6	K562	blood:
8	chr4:77165685..77168329-chr4:77226063..77227716,2	MCF-7	breast:
9	chr4:77171623..77174207-chr4:77177725..77179646,2	MCF-7	breast:
10	chr4:77069302..77071113-chr4:77170408..77173032,2	MCF-7	breast:
11	chr4:77154267..77157230-chr4:77166961..77169632,3	MCF-7	breast:
12	chr4:77171768..77173922-chr4:77226650..77228948,4	MCF-7	breast:
13	chr4:77133904..77135705-chr4:77183809..77185526,2	MCF-7	breast:
14	chr4:77185052..77186767-chr4:77189879..77191604,2	K562	blood:
15	chr4:77165064..77167493-chr4:77174521..77177235,2	K562	blood:
16	chr4:77156486..77158714-chr4:77178616..77181802,3	MCF-7	breast:
17	chr4:77101090..77101653-chr4:77166939..77167466,2	MCF-7	breast:
18	chr4:77100761..77101387-chr4:77166867..77167817,2	MCF-7	breast:
19	chr4:77154984..77156976-chr4:77172946..77174616,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STBD1-1	chr4:77177331-77177613	ENSG00000248325.1
2	lnc-STBD1-2	chr4:77172853-77172973	NONHSAT096993
3	lnc-SCARB2-1	chr4:77172297-77172990	NONHSAT096992
4	lnc-STBD1-2	chr4:77184857-77184996	NONHSAT096993

No data

Variant related genes	Relation type
FAM47E-STBD1	TF binding region
ENSG00000272414	TF binding region
FAM47E	TF binding region
FAM47E-STBD1	CpG island
ENSG00000272414	CpG island
FAM47E	CpG island
ENSG00000189157	chromatin interactions
ENSG00000138750	chromatin interactions
ENSG00000272414	chromatin interactions
ENSG00000138760	chromatin interactions
ENSG00000118804	chromatin interactions

Extended variants
information (count: 703 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:703 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4859643	chr4:77164549-77164550	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs368210240	chr4:77165686-77165687	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs71212407	chr4:77165687-77165688	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs34115941	chr4:77165754-77165755	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs376870952	chr4:77165755-77165756	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs570256843	chr4:77165786-77165787	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs537819355	chr4:77165804-77165805	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs192631681	chr4:77165871-77165872	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs4859645	chr4:77165893-77165894	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs565398845	chr4:77165982-77165983	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs34521402	chr4:77166008-77166009	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs4859646	chr4:77166011-77166012	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs553495338	chr4:77166102-77166103	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs78770313	chr4:77166111-77166112	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs576590769	chr4:77166116-77166117	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs189137325	chr4:77166145-77166146	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs374865118	chr4:77166223-77166224	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs368352268	chr4:77166260-77166261	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs140900719	chr4:77166284-77166285	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs576276991	chr4:77166285-77166286	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs13328061	chr4:77166362-77166363	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs561913390	chr4:77166376-77166377	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs527735003	chr4:77166382-77166383	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs547903364	chr4:77166402-77166403	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs116674622	chr4:77166490-77166491	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs28459239	chr4:77166493-77166494	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs146816234	chr4:77166584-77166585	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs550199186	chr4:77166588-77166589	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs148831142	chr4:77166598-77166599	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs7670989	chr4:77166624-77166625	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs180704403	chr4:77166639-77166640	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs368454007	chr4:77166643-77166644	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs549676848	chr4:77166675-77166676	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs567714411	chr4:77166704-77166705	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs533581846	chr4:77166712-77166713	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs74526079	chr4:77166740-77166741	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs368537152	chr4:77166741-77166742	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs377250193	chr4:77166762-77166763	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs72858586	chr4:77166858-77166859	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs567186193	chr4:77166873-77166874	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs72858588	chr4:77166938-77166939	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs111340243	chr4:77167099-77167100	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs556072143	chr4:77167145-77167146	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs576215198	chr4:77167155-77167156	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs568469495	chr4:77167156-77167157	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs537287140	chr4:77167216-77167217	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs1348206	chr4:77167242-77167243	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs572430521	chr4:77167278-77167279	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs72858593	chr4:77167286-77167287	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs186449544	chr4:77167312-77167313	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
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
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	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
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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:445 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:77166200-77167600	Enhancers	Skeletal Muscle Female	skeletal muscle
2	chr4:77166400-77167000	Enhancers	Psoas Muscle	Psoas
3	chr4:77166600-77167000	Enhancers	Brain Angular Gyrus	brain
4	chr4:77166800-77167600	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr4:77167600-77171800	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr4:77170800-77171600	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr4:77171400-77171800	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr4:77171400-77172000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
9	chr4:77171600-77172000	Enhancers	Fetal Intestine Large	intestine
10	chr4:77171600-77173800	Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr4:77171800-77172000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
12	chr4:77171800-77172000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
13	chr4:77171800-77172000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
14	chr4:77171800-77172000	Enhancers	Brain Cingulate Gyrus	brain
15	chr4:77171800-77172000	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr4:77171800-77172200	Active TSS	Brain Hippocampus Middle	brain
17	chr4:77171800-77172200	Enhancers	Stomach Mucosa	stomach
18	chr4:77171800-77172200	Bivalent Enhancer	HepG2	liver
19	chr4:77172000-77172200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
20	chr4:77172000-77172200	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr4:77172000-77172200	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr4:77172000-77172200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr4:77172000-77172200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr4:77172000-77172200	Enhancers	Adipose Nuclei	Adipose
25	chr4:77172000-77172200	Enhancers	Liver	Liver
26	chr4:77172000-77172200	Active TSS	Brain Angular Gyrus	brain
27	chr4:77172000-77172200	Enhancers	Brain Substantia Nigra	brain
28	chr4:77172000-77172200	Active TSS	Duodenum Mucosa	Duodenum
29	chr4:77172000-77172200	Enhancers	Duodenum Smooth Muscle	Duodenum
30	chr4:77172000-77172200	Enhancers	Fetal Heart	heart
31	chr4:77172000-77172200	Enhancers	Fetal Intestine Small	intestine
32	chr4:77172000-77172200	Enhancers	Placenta	Placenta
33	chr4:77172000-77172200	Active TSS	Rectal Mucosa Donor 31	rectum
34	chr4:77172000-77172200	Enhancers	Rectal Smooth Muscle	rectum
35	chr4:77172000-77172200	Enhancers	Stomach Smooth Muscle	stomach
36	chr4:77172000-77172200	Bivalent Enhancer	HMEC	breast
37	chr4:77172000-77172400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
38	chr4:77172000-77172400	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
39	chr4:77172000-77172400	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
40	chr4:77172000-77172400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr4:77172000-77172400	Flanking Active TSS	Brain Cingulate Gyrus	brain
42	chr4:77172000-77172600	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
43	chr4:77172000-77172600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
44	chr4:77172000-77172600	Bivalent/Poised TSS	Fetal Stomach	stomach
45	chr4:77172000-77172600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
46	chr4:77172000-77172600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
47	chr4:77172000-77173000	Active TSS	Psoas Muscle	Psoas
48	chr4:77172000-77173400	Active TSS	Brain Inferior Temporal Lobe	brain
49	chr4:77172000-77173600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
50	chr4:77172000-77173600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle

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