EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS091-14203 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr14:103574860-103576360 
Target genes
Number: 8             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2274685chr14103575070hg19
TF binding sites/motifs
Number: 31             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr14:103575550-103575571CTCCCTCCCTCCCTCTCCACC-6.31
ZNF263MA0528.1chr14:103575587-103575608CTCCCTCCCTCCCTCTCCACC-6.31
ZNF263MA0528.1chr14:103575624-103575645CTCCCTCCCTCCCTCTCCACC-6.31
ZNF263MA0528.1chr14:103575877-103575898CTCCCTCCCTCCCTCTCCACC-6.31
ZNF263MA0528.1chr14:103576022-103576043CTCCCTCCCTCCCTCTCCACC-6.31
ZNF263MA0528.1chr14:103575481-103575502CCTCCCTCCCTCTCCACCACC-6.37
ZNF263MA0528.1chr14:103575631-103575652CCTCCCTCTCCACCCTGCCCC-6.46
ZNF263MA0528.1chr14:103575667-103575688CCTCCCTCTCCACCCTGCCCC-6.46
ZNF263MA0528.1chr14:103575703-103575724CCTCCCTCTCCACCCTGCCCC-6.46
ZNF263MA0528.1chr14:103575739-103575760CCTCCCTCTCCACCCTGCCCC-6.46
ZNF263MA0528.1chr14:103575775-103575796CCTCCCTCTCCACCCTGCCCC-6.46
ZNF263MA0528.1chr14:103575811-103575832CCTCCCTCTCCACCCTGCCCC-6.46
ZNF263MA0528.1chr14:103575884-103575905CCTCCCTCTCCACCCTGCCCC-6.46
ZNF263MA0528.1chr14:103575920-103575941CCTCCCTCTCCACCCTGCCCC-6.46
ZNF263MA0528.1chr14:103575956-103575977CCTCCCTCTCCACCCTGCCCC-6.46
ZNF263MA0528.1chr14:103575992-103576013CCTCCCTCTCCACCCTGCCCC-6.46
ZNF263MA0528.1chr14:103575660-103575681CCTCCTCCCTCCCTCTCCACC-6.48
ZNF263MA0528.1chr14:103575696-103575717CCTCCTCCCTCCCTCTCCACC-6.48
ZNF263MA0528.1chr14:103575732-103575753CCTCCTCCCTCCCTCTCCACC-6.48
ZNF263MA0528.1chr14:103575768-103575789CCTCCTCCCTCCCTCTCCACC-6.48
ZNF263MA0528.1chr14:103575804-103575825CCTCCTCCCTCCCTCTCCACC-6.48
ZNF263MA0528.1chr14:103575840-103575861CCTCCTCCCTCCCTCTCCACC-6.48
ZNF263MA0528.1chr14:103575913-103575934CCTCCTCCCTCCCTCTCCACC-6.48
ZNF263MA0528.1chr14:103575949-103575970CCTCCTCCCTCCCTCTCCACC-6.48
ZNF263MA0528.1chr14:103575985-103576006CCTCCTCCCTCCCTCTCCACC-6.48
ZNF263MA0528.1chr14:103575544-103575565GTCTCCCTCCCTCCCTCCCTC-6.4
ZNF263MA0528.1chr14:103575581-103575602GTCTCCCTCCCTCCCTCCCTC-6.4
ZNF263MA0528.1chr14:103575618-103575639GTCTCCCTCCCTCCCTCCCTC-6.4
ZNF263MA0528.1chr14:103575871-103575892GTCTCCCTCCCTCCCTCCCTC-6.4
ZNF263MA0528.1chr14:103576016-103576037GTCTCCCTCCCTCCCTCCCTC-6.4
ZNF263MA0528.1chr14:103575478-103575499CCCCCTCCCTCCCTCTCCACC-6.76
Number of super-enhancer constituents: 18             
IDCoordinateTissue/cell
SE_01277chr14:103576034-103578018Adrenal_Gland
SE_09890chr14:103574484-103575477CD14
SE_27118chr14:103575947-103577812Esophagus
SE_31686chr14:103574356-103575539Gastric
SE_31686chr14:103575968-103579658Gastric
SE_33976chr14:103576005-103579434HCC1954
SE_34594chr14:103574068-103579771HCT-116
SE_34982chr14:103574382-103575670HeLa
SE_34982chr14:103575825-103580066HeLa
SE_50540chr14:103574385-103575539Sigmoid_Colon
SE_50540chr14:103575975-103580334Sigmoid_Colon
SE_53185chr14:103574395-103575507Small_Intestine
SE_53185chr14:103575969-103580153Small_Intestine
SE_53645chr14:103574524-103575634Spleen
SE_53645chr14:103575931-103579122Spleen
SE_59574chr14:103557209-103581735Ly3
SE_65696chr14:103574005-103575678Pancreatic_islets
SE_65696chr14:103575967-103579278Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr14103575159103575514
Number: 1             
IDChromosomeStartEnd
GH14I103107chr14103573439103580181
Enhancer Sequence
ACCCCACCTG CTTCCACTAG CTTCCTACCA GAGCTTCAGG GCCAAGGGGG CTGGTATTGG 60
AGCAACCCCA GCCCAGACCT GACTGCCCAG GGGCCTGAAG ACCAGAGGCA GGAGGTAGGC 120
CTTGGACCCT CAGACCCTCA AGGCTGGAGG GGGAATGGAG AGAGCCCCTT CTCCTAATCT 180
GCTCTTGGCC ATCCTCCATC AGCCCCACCA GGGGTGGGCA CGCCTCCAGT CCTGGAATCT 240
GAGGGGGAGG CGGACCCCCC ACCCCTGGGG AGAAAGCCCT CTCTGAAAGC CAGGGGATTC 300
TGAGACCTGG TCAGGAGGAA GGAGGTTTTG ATCCCGGGTT GTGCTGGGGG GTCGGTGAGT 360
CATCCAAGCC TTTGGAAATC CCAGCTCGAA TCTCTCCAAG TCCATTCTTT TGGAGATTCT 420
GGGATGTGGA GCTCACAGAA AGCCCCTGGT TCATCCCCTT CCCCAGGCCA CCCTGCCATG 480
GGGTGGGGAA GGATTCCCCA TCCCCAGCAG GCCTGTCTTC CAGGCTGTGG CTCAGAGAGA 540
GTGGCCCTTA CATCACCCTG GGAGTTCCCC TCCAACTACT CCCCAACCCC GTTGGCCCCG 600
TCACCCGCAG CTGCATCACC CCCTCCCTCC CTCTCCACCA CCTGTCCCCC GGTCTCCCTC 660
TCTCCCTCGC CACCCTGTCC CCATGTCTCC CTCCCTCCCT CCCTCTCCAC CCTGTCCCCG 720
TGTCTCCCTC CCTCCCTCCC TCTCCACCCT GTCCCCATGT CTCCCTCCCT CCCTCCCTCT 780
CCACCCTGCC CCCATGTCTC CCTCCTCCCT CCCTCTCCAC CCTGCCCCCA TGTCTCCCTC 840
CTCCCTCCCT CTCCACCCTG CCCCCATGTC TCCCTCCTCC CTCCCTCTCC ACCCTGCCCC 900
CATGTCTCCC TCCTCCCTCC CTCTCCACCC TGCCCCCATG TCTCCCTCCT CCCTCCCTCT 960
CCACCCTGCC CCCATGTCTC CCTCCTCCCT CCCTCTCCAC CCTGTCCCCA TGTCTCCCTC 1020
CCTCCCTCCC TCTCCACCCT GCCCCCATGT CTCCCTCCTC CCTCCCTCTC CACCCTGCCC 1080
CCATGTCTCC CTCCTCCCTC CCTCTCCACC CTGCCCCCAT GTCTCCCTCC TCCCTCCCTC 1140
TCCACCCTGC CCCCATGTCT CCCTCCCTCC CTCCCTCTCC ACCCTGTCCC TGGGTCTCCC 1200
TCTCTCTCCA GCCTGGGTCT CTCCACCCGG TCCCCAGGTC TCCCTCCACG CCTTTGCGTG 1260
GGCTCTTTCC CACTCTGCAC ACCCCTCTCC TGTGCCCCTT CAAGCCCAGC TATGGTGTCC 1320
CCCAGGCCCA CGCCCTGCCC CCTCCCCCAG CACAGCTCTT CCTGGCCTCA GTCAATCTGA 1380
CCTCCCTGAC CATCCTGGAA TGCAGAGTGA CTCATACTAA CTCCCAAGCC CGTGGGTTCG 1440
CCTCATGCTG GGGCTGGGGG TGTTGCGGAG GTGTAGGTCT GCAGTGAGTG CCCGCATGTC 1500