EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS133-15041 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr19:13111910-13114420 
Target genes
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs10411958chr1913113641hg19
TF binding sites/motifs
Number: 14             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr19:13113041-13113059CCCTCCTCCCCTCCTCCC-6.34
PLAG1MA0163.1chr19:13113593-13113607CCCCACTGGGCCCC-6.36
RREB1MA0073.1chr19:13114378-13114398ACACAAAACACCCCACACAC+6.58
ZNF263MA0528.1chr19:13113187-13113208CCCCCCTTCCTCACCACCTCC-6.06
ZNF263MA0528.1chr19:13113010-13113031TTCTCTCTCTCTCTTTCCTCC-6.09
ZNF263MA0528.1chr19:13113024-13113045TTCCTCCCTCTCTCCTCCCCT-6.1
ZNF263MA0528.1chr19:13113013-13113034TCTCTCTCTCTTTCCTCCCTC-6.71
ZNF263MA0528.1chr19:13113032-13113053TCTCTCCTCCCCTCCTCCCCT-6.81
ZNF263MA0528.1chr19:13113046-13113067CTCCCCTCCTCCCGCTCCCTC-6.97
ZNF263MA0528.1chr19:13113179-13113200TCCCCAACCCCCCCTTCCTCA-6
ZNF263MA0528.1chr19:13113021-13113042TCTTTCCTCCCTCTCTCCTCC-7.11
ZNF263MA0528.1chr19:13113066-13113087CTCTCCCTCTCTCTCTCCTCC-7.55
ZNF263MA0528.1chr19:13113037-13113058CCTCCCCTCCTCCCCTCCTCC-8.34
ZNF263MA0528.1chr19:13113029-13113050CCCTCTCTCCTCCCCTCCTCC-8.3
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_00024chr19:13106663-13152679Adipose_Nuclei
SE_01540chr19:13110142-13115698Aorta
SE_02988chr19:13111642-13113363Bladder
SE_02988chr19:13113437-13114106Bladder
SE_03137chr19:13111167-13113446Brain_Angular_Gyrus
SE_03137chr19:13113464-13114654Brain_Angular_Gyrus
SE_03859chr19:13110392-13115719Brain_Anterior_Caudate
SE_05694chr19:13106749-13121974Brain_Cingulate_Gyrus
SE_05829chr19:13106701-13152645Brain_Hippocampus_Middle
SE_06678chr19:13106696-13115944Brain_Hippocampus_Middle_150
SE_07717chr19:13106671-13121243Brain_Inferior_Temporal_Lobe
SE_08780chr19:13111910-13112642Brain_Mid_Frontal_Lobe
SE_08780chr19:13113611-13114524Brain_Mid_Frontal_Lobe
SE_26006chr19:13110962-13113463Duodenum_Smooth_Muscle
SE_26520chr19:13104240-13115760Esophagus
SE_29659chr19:13111392-13114578Fetal_Muscle
SE_31390chr19:13111381-13115785Gastric
SE_40665chr19:13111809-13114684Left_Ventricle
SE_41557chr19:13110243-13114586LNCaP
SE_44148chr19:13110197-13114666NHDF-Ad
SE_44758chr19:13111492-13114166NHLF
SE_45899chr19:13112164-13113128Osteoblasts
SE_46652chr19:13111347-13114316Ovary
SE_48559chr19:13110197-13114606Right_Atrium
SE_50434chr19:13111382-13114599Sigmoid_Colon
SE_51076chr19:13106668-13152566Skeletal_Muscle
SE_53207chr19:13111453-13113204Small_Intestine
SE_54519chr19:13106712-13122633Stomach_Smooth_Muscle
SE_67980chr19:13100968-13183275TC32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr191311344713113871
Number: 1             
IDChromosomeStartEnd
GH19I013000chr191311104013114468
Enhancer Sequence
GGGTGGGGAA AAGGAGGGGG GTGTCTTAAT TTTCTTGCCC CCAAAGCCCT GGATGTGGGG 60
GCAAGTGGGC CAGGAGGACA GCTGTGAGCC ACTATCTGGG TTCTCCCAGA TCGGTGTGCA 120
TGTTAATCGG CATGTCAGGC CTCAGAGCCA CCATTTTCCC GAGGATGTCT GTGTGGCAGC 180
GTGTGTCTGC CCGGGTCCCT CTCCATGCCT CTCCATGTCT CCCAGCGTCC ATCACTGGGT 240
GCTACCTGCA TGTGACTCCA CGGATCATCG CACGCCCTGT CTCTTGTGTA TTTGGTAGTG 300
GGGGTCGGGG AGCGTGCCAC CATGCGTGTC AGTGTGCCGG ATGTAGTCTC TGTGTCACGG 360
TGGCGCTGCG CACGTCAACG GGTATTGGTG TACCGGTCAC CATCTTTGTA TCTGCGCTTT 420
GTATCTGGGG TGACAGTGTC CCAGCGACAT GCGTCACATC TACAGCAGTG TTTTTCTGGG 480
TGTCTGTGCG TCACGGCAAA GAGTGTATCC GTGTGTCTCA CACACGTGTT GGCCTGTCCG 540
TGTCAACTTG TGTCCACATA CGTGTCAACG CACGTGTCTC CAGTGTCATC ACCCTCATAT 600
CACTGTGCCT CCTGAGCTTG TCCCCGTGAC AATCACTGTG GGTCTCACCC CACGGGCGCC 660
TCTCCTGGGC ATTCCCTTGG CCTCCGAGCA CCATGTGAGA TGCCTGCTAT GGCGGCCGGG 720
CAAGCGGCTG GGAGCGGGCT GGCTGCTCAG TCCCTTCCCA TGAGGTTGAG CGGCCGCAGT 780
GGCCTTGCTG GGGGCCCCGC CCGTGCCCCT GGCCTGGCGT GGACAGAAGC CCGTTGTGCG 840
GCAGCGAGGT GCGGGCGTGT GTTCGGGCCG CCCACAGGCC TCCCTCTGTC TGCCCGGCGC 900
ACATTGATCT TGGCTTCTGC CTGTGTCCGT TCTAGCCTGG CCAGCTGGGT GTCCGGCTGT 960
CTCCGTGGGC CTGAGCCCAC TATCCCCGCT GCCCCCACAG CCAGGCAGGC CCTGGGCCCC 1020
ACACCCCTGG GCCACCCGCC ATCCCTCCGA GGCTCTGAGG GCGCGGATTT GGAAACTGAG 1080
GTCCCCCCTT CTTTCCCCCT TTCTCTCTCT CTCTTTCCTC CCTCTCTCCT CCCCTCCTCC 1140
CCTCCTCCCG CTCCCTCTCT CCCTCTCTCT CTCCTCCTGC CAAACGCGTC TTGGCTCCGT 1200
CTGAATATCT CTCCTCCTCG ATTTTTGGCT CCAGCTCTGG GCGCGTTCAC TAAAGGAAGA 1260
AGGGCTAGCT CCCCAACCCC CCCTTCCTCA CCACCTCCCC CCTCCCGAGG AGCCCCTCTG 1320
AGGGCGGGAG TGGCCTCGTG CAGGGGCCTG GGCCCCCTGA GTGGGCTTGG CCAGGGGGGC 1380
ACAGGCCTGG CGGGTGAGGG AACAGGGTGG ACAGGGCCTG GCAGCCAGAG GGAGGCAATG 1440
GGCAGGGTGA CTGAGCTGCC CGGCGGGGCG GGCGGGCAGG GAGGGGTCGG GGGCACGGAG 1500
CTGGGGTGTC TGGCTTCTGG TGGGGCTGGC AGGCCTCTGT GAGGCGCAGC TGTGCCCAGA 1560
ACTCCAAGTT GCGTTTGCCA CCACTACCGA TGTGGCTGCG CCAGCCAGGG AGGGGAGGCG 1620
GGTAGCGGGC ACTGCGGCGC TCTGCAGCCA ATCGGAAGCC GGGGTTGCAC TGGGGAGCTC 1680
TCCCCCCACT GGGCCCCACC CTGAGGGGAG CCGGGGGTGG TGGCCAGCAG TGGGCAGGGG 1740
GCAGTGCCCA CCACCATCGC CAAGGACCCT GCCCCCTCAG CTGAAGCTCA GTGCCAGCCT 1800
TCCTGGCACA GATCGGGCAA GAGCGGGGAT CTGTCTGTCC CCACCTGAAT CTGTGTGAGC 1860
CAAGCTGGAG GAAAGGACAG CATGGAGGTG CACCCGACCC CCCTGGGCCT TTTAGTCCAA 1920
GGCAGGCAGG AGCTAGGGAT GGGTTCCAAA TTATCCAGGT GGTTCCGTCC AAATATCGGC 1980
TTCGGTCGAA TCATCTTGGG GAGTTGGGGG GGGGTTTATT CCGGGTCCAT CTCACACAAA 2040
GTCACACACT CTCACTGGCA CATGCGGGCA CAAAGAATCA CGCTGACACA CACTGGCATG 2100
CTGCACCTCC CTCAATCAAA CAGACACAGG CGTCCCCATA CAAAGAATCT TGCCCTCACT 2160
CACAGACACC TTGAGGCACC CGGCCACACC CGAACACATC GATGCGGCAT TACACACTCA 2220
GGGACGTGCA TGTGGGTGCA GACACACGGG ACACGCGCAG TCACACGATC ACATGCCATG 2280
AAGCACACAG CACAGACACA GGCTCTGCCA CCGTCAAATG CAGCCCCACA GGCACAGCTA 2340
GAAACACACA GCACACACAC TCAGTCATAA TGTCAGTGCC CAAAACACAC ACATGAGCAC 2400
CGATACACCC GCACATGCCA CCAAGCACAC AGGTACATGC ACATGCATGC AATAACACGC 2460
TCTCAGACAC ACAAAACACC CCACACACTC CCTAACCCAG TGTCACCCAC 2510