Variant report

Variant	esv1795247
Chromosome Location	chr4:69491911-69567590
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:442)
CpG islands
(count:366)
Chromatin interactive
region (count:2)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:442 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:69521827-69522720	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:69524230-69524826	HepG2	liver:	n/a	n/a
3	ATF1	chr4:69559343-69559671	K562	blood:	n/a	n/a
4	BATF	chr4:69523003-69523215	GM12878	blood:	n/a	n/a
5	BATF	chr4:69522977-69523278	GM12878	blood:	n/a	n/a
6	BATF	chr4:69538989-69539205	GM12878	blood:	n/a	n/a
7	BCL11A	chr4:69523069-69523272	GM12878	blood:	n/a	n/a
8	BCL3	chr4:69536262-69536632	A549	lung:	n/a	n/a
9	BHLHE40	chr4:69522248-69522562	GM12878	blood:	n/a	n/a
10	BHLHE40	chr4:69559209-69559522	K562	blood:	n/a	n/a
11	CEBPB	chr4:69536204-69536567	A549	lung:	n/a	chr4:69536341-69536354
12	CEBPB	chr4:69536198-69536502	MCF-7	breast:	n/a	chr4:69536341-69536354
13	CEBPB	chr4:69536174-69536504	A549	lung:	n/a	chr4:69536341-69536354
14	CEBPB	chr4:69536277-69536474	HepG2	liver:	n/a	chr4:69536341-69536354
15	CEBPB	chr4:69530297-69530431	A549	lung:	n/a	chr4:69530340-69530351
16	CEBPB	chr4:69530299-69530470	HepG2	liver:	n/a	chr4:69530340-69530351
17	CTCF	chr4:69538958-69539150	A549	lung:	n/a	n/a
18	CTCF	chr4:69537020-69537170	GM06990	blood:	n/a	n/a
19	CTCF	chr4:69537117-69537216	GM10248	blood:	n/a	n/a
20	CTCF	chr4:69537020-69537170	HMEC	breast:	n/a	n/a
21	CTCF	chr4:69537096-69537228	GM12892	blood:	n/a	n/a
22	CTCF	chr4:69539830-69539892	GM13977	blood:	n/a	n/a
23	CTCF	chr4:69537760-69537910	GM12873	blood:	n/a	n/a
24	CTCF	chr4:69539000-69539150	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr4:69523122-69523163	K562	blood:	n/a	n/a
26	CTCF	chr4:69537087-69537228	K562	blood:	n/a	n/a
27	CTCF	chr4:69538977-69539098	MCF-7	breast:	n/a	n/a
28	CTCF	chr4:69537020-69537170	SAEC	small airway:	n/a	n/a
29	CTCF	chr4:69522940-69523090	MCF-7	breast:	n/a	n/a
30	CTCF	chr4:69538980-69539130	GM12872	blood:	n/a	n/a
31	CTCF	chr4:69538977-69539100	NHEK	skin:	n/a	n/a
32	CTCF	chr4:69523015-69523281	GM19238	blood:	n/a	n/a
33	CTCF	chr4:69537057-69537265	MCF-7	breast:	n/a	n/a
34	CTCF	chr4:69537020-69537170	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr4:69537779-69537857	MCF-7	breast:	n/a	n/a
36	CTCF	chr4:69539680-69539830	GM12873	blood:	n/a	n/a
37	CTCF	chr4:69537765-69537845	MCF-7	breast:	n/a	n/a
38	CTCF	chr4:69539060-69539210	GM12875	blood:	n/a	n/a
39	CTCF	chr4:69537020-69537170	HepG2	liver:	n/a	n/a
40	CTCF	chr4:69523080-69523234	GM12891	blood:	n/a	n/a
41	CTCF	chr4:69538954-69539224	K562	blood:	n/a	n/a
42	CTCF	chr4:69537674-69537844	K562	blood:	n/a	n/a
43	CTCF	chr4:69539000-69539150	GM06990	blood:	n/a	n/a
44	CTCF	chr4:69537040-69537190	GM12873	blood:	n/a	n/a
45	CTCF	chr4:69538992-69539099	HepG2	liver:	n/a	n/a
46	CTCF	chr4:69537020-69537170	GM12875	blood:	n/a	n/a
47	CTCF	chr4:69537020-69537170	GM12874	blood:	n/a	n/a
48	CTCF	chr4:69537020-69537170	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr4:69538980-69539130	GM12865	blood:	n/a	n/a
50	CTCF	chr4:69537097-69537207	Fibrobl	skin:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69514031-69514081	HCT-116	colon:	n/a
2	chr4:69514031-69514081	AG04449	skin:	fetal
3	chr4:69514031-69514081	BE2_C	brain:	n/a
4	chr4:69537806-69537856	AG10803	skin:	n/a
5	chr4:69537589-69537639	GM19239	blood:	n/a
6	chr4:69537806-69537856	HRE	kidney:	n/a
7	chr4:69537589-69537639	HCT-116	colon:	n/a
8	chr4:69537806-69537856	Jurkat	blood:	n/a
9	chr4:69537826-69537876	T-47D	breast:	n/a
10	chr4:69537806-69537856	Caco-2	colon:	n/a
11	chr4:69537826-69537876	PFSK-1	brain:	n/a
12	chr4:69537826-69537876	SK-N-SH_RA	brain:	n/a
13	chr4:69537806-69537856	HUVEC	blood vessel:	n/a
14	chr4:69514031-69514081	SAEC	small airway:	n/a
15	chr4:69514031-69514081	H1-hESC	embryonic stem cell:	embryo
16	chr4:69537589-69537639	AG04449	skin:	fetal
17	chr4:69536319-69536369	SK-N-MC	brain:	n/a
18	chr4:69537806-69537856	PANC-1	pancreas:	n/a
19	chr4:69522639-69522689	PFSK-1	brain:	n/a
20	chr4:69537826-69537876	HUVEC	blood vessel:	n/a
21	chr4:69537589-69537639	NB4	blood:	n/a
22	chr4:69522639-69522689	BJ	skin:	n/a
23	chr4:69537589-69537639	HRCEpiC	kidney:	n/a
24	chr4:69537589-69537639	HepG2	liver:	n/a
25	chr4:69537826-69537876	HCT-116	colon:	n/a
26	chr4:69522639-69522689	HL-60	blood:	n/a
27	chr4:69514031-69514081	GM12892	blood:	n/a
28	chr4:69536319-69536369	GM12891	blood:	n/a
29	chr4:69522639-69522689	HIPEpiC	eye:	n/a
30	chr4:69537826-69537876	NHBE	bronchial:	n/a
31	chr4:69537826-69537876	LNCaP	prostate:	n/a
32	chr4:69536319-69536369	PFSK-1	brain:	n/a
33	chr4:69537826-69537876	GM19239	blood:	n/a
34	chr4:69514031-69514081	HepG2	liver:	n/a
35	chr4:69536319-69536369	Jurkat	blood:	n/a
36	chr4:69537806-69537856	NHDF-neo	bronchial:	n/a
37	chr4:69536319-69536369	NH-A	brain:	n/a
38	chr4:69522639-69522689	PrEC	prostate:	n/a
39	chr4:69514031-69514081	HEEpiC	esophagus:	n/a
40	chr4:69514031-69514081	PFSK-1	brain:	n/a
41	chr4:69536319-69536369	SKMC	muscle:	n/a
42	chr4:69537589-69537639	HAEpiC	amniotic membrane:	n/a
43	chr4:69536319-69536369	AG10803	skin:	n/a
44	chr4:69536319-69536369	HPAEpiC	pulmonary alveolar:	n/a
45	chr4:69537806-69537856	H1-hESC	embryonic stem cell:	embryo
46	chr4:69514031-69514081	HRCEpiC	kidney:	n/a
47	chr4:69537589-69537639	HNPCEpiC	eye:	n/a
48	chr4:69522639-69522689	AG09319	gingival:	n/a
49	chr4:69536319-69536369	HIPEpiC	eye:	n/a
50	chr4:69537806-69537856	IMR90	lung:	fetal

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:73105975..73106777-chr4:69561197..69562068,2	MCF-7	breast:
2	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B15-2	chr4:69492565-69492700	NONHSAT096737
2	lnc-UGT2B15-2	chr4:69493903-69494617	NONHSAT096737

No data

Variant related genes	Relation type
ENSG00000251074	TF binding region
UGT2B15	TF binding region
ENSG00000251074	CpG island
UGT2B15	CpG island

Extended variants
information (count: 2289 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2289 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545339079	chr4:69491924-69491925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs565259056	chr4:69491936-69491937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191700605	chr4:69491976-69491977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149681278	chr4:69491981-69491982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs145506216	chr4:69491988-69491989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs530220769	chr4:69491993-69491994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs549991906	chr4:69492001-69492002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs181809954	chr4:69492007-69492008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs200964946	chr4:69492017-69492018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs376244484	chr4:69492023-69492024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532428051	chr4:69492029-69492030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148832263	chr4:69492050-69492051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs143438823	chr4:69492078-69492079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs534297039	chr4:69492099-69492100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533172471	chr4:69492106-69492107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs534664356	chr4:69492136-69492137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185977392	chr4:69492151-69492152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs147646035	chr4:69492173-69492174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536788475	chr4:69492189-69492190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs556334132	chr4:69492190-69492191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs569942544	chr4:69492206-69492207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577616925	chr4:69492219-69492220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs538929225	chr4:69492238-69492239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs190829676	chr4:69492272-69492273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs565653016	chr4:69492300-69492301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs36016278	chr4:69492319-69492320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs4443356	chr4:69492419-69492420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs554988878	chr4:69492438-69492439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542436514	chr4:69492443-69492444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs35047063	chr4:69492446-69492447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs543963021	chr4:69492448-69492449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs563458762	chr4:69492451-69492452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs532313412	chr4:69492452-69492453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs546003754	chr4:69492454-69492455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs559340628	chr4:69492455-69492456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs141254182	chr4:69492474-69492475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs150441832	chr4:69492498-69492499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs573011397	chr4:69492538-69492539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs138199685	chr4:69492549-69492550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs4455492	chr4:69492552-69492553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs538828031	chr4:69492554-69492555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs35785990	chr4:69492555-69492556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs371953043	chr4:69492561-69492562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs566202544	chr4:69492593-69492594	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs535375696	chr4:69492600-69492601	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs183424612	chr4:69492609-69492610	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs140192333	chr4:69492618-69492619	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs186636823	chr4:69492624-69492625	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs557465100	chr4:69492626-69492627	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs386675592	chr4:69492629-69492630	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
Oral cancer	21386901	CNVD
Alcoholism	21790672	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:136 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69485400-69501800	Weak transcription	Liver	Liver
2	chr4:69490400-69492200	Enhancers	Fetal Heart	heart
3	chr4:69491800-69492600	Enhancers	HepG2	liver
4	chr4:69495000-69497400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr4:69495800-69496600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr4:69496000-69496400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr4:69496000-69496400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr4:69496200-69496600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr4:69501800-69502400	ZNF genes & repeats	Liver	Liver
10	chr4:69502400-69504200	Weak transcription	Liver	Liver
11	chr4:69504200-69505800	ZNF genes & repeats	Liver	Liver
12	chr4:69511400-69514200	ZNF genes & repeats	Liver	Liver
13	chr4:69511600-69512000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr4:69511600-69513000	ZNF genes & repeats	Pancreas	Pancrea
15	chr4:69513000-69522800	Weak transcription	Pancreas	Pancrea
16	chr4:69514200-69516000	Strong transcription	Liver	Liver
17	chr4:69515800-69518200	Weak transcription	Psoas Muscle	Psoas
18	chr4:69516000-69516600	ZNF genes & repeats	Liver	Liver
19	chr4:69516600-69521800	Strong transcription	Liver	Liver
20	chr4:69519800-69522200	Enhancers	NHEK	skin
21	chr4:69519800-69523000	Enhancers	HMEC	breast
22	chr4:69520400-69521800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr4:69520400-69523000	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr4:69520400-69523000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr4:69520800-69521800	Enhancers	A549	lung
26	chr4:69520800-69521800	Enhancers	HepG2	liver
27	chr4:69521000-69522600	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr4:69521200-69521600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr4:69521200-69522600	Enhancers	Rectal Mucosa Donor 31	rectum
30	chr4:69521200-69522600	Enhancers	Stomach Mucosa	stomach
31	chr4:69521200-69522800	Enhancers	H9 Cell Line	embryonic stem cell
32	chr4:69521200-69522800	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr4:69521200-69522800	Enhancers	Fetal Intestine Large	intestine
34	chr4:69521400-69522200	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr4:69521400-69522800	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr4:69521600-69522000	Enhancers	Rectal Mucosa Donor 29	rectum
37	chr4:69521600-69522600	Enhancers	H1 Cell Line	embryonic stem cell
38	chr4:69521600-69522800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr4:69521800-69522000	Genic enhancers	Liver	Liver
40	chr4:69521800-69522000	Enhancers	Fetal Intestine Small	intestine
41	chr4:69521800-69522000	Flanking Active TSS	A549	lung
42	chr4:69521800-69522000	Flanking Active TSS	HepG2	liver
43	chr4:69521800-69522200	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr4:69521800-69522400	Enhancers	Duodenum Mucosa	Duodenum
45	chr4:69521800-69522600	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr4:69521800-69522800	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr4:69521800-69523000	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr4:69522000-69522200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
49	chr4:69522000-69522400	Active TSS	A549	lung
50	chr4:69522000-69522400	Active TSS	GM12878-XiMat	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links