EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS060-32978 
Organism
Homo sapiens 
Tissue/cell
GM12891 
Coordinate
chr8:11275270-11276740 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2002030chr811276542hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ESR2MA0258.2chr8:11275577-11275592GGGGCTTTGTGACCT-6.02
RARA(var.2)MA0730.1chr8:11275493-11275510AGGTCGACCAGAGGTCA+6.65
SOX10MA0442.2chr8:11276305-11276316TGCTTTGTTTT-6.02
STAT1MA0137.3chr8:11275322-11275333TTTCTGGGAAA+6.02
STAT3MA0144.2chr8:11275322-11275333TTTCTGGGAAA+6.32
Stat4MA0518.1chr8:11275322-11275336TTTCTGGGAAAGGG+6.56
ZNF263MA0528.1chr8:11276048-11276069CCTTTATCTCCTGCCTCCTCC-6.55
Number of super-enhancer constituents: 3             
IDCoordinateTissue/cell
SE_58515chr8:11271776-11367112Ly1
SE_60559chr8:11246636-11318640DHL6
SE_65314chr8:11275329-11276524Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr81127635111276570
chr81127658311276682
chr81127530411276094
Number: 1             
IDChromosomeStartEnd
GH08I011416chr81127409711276396
Enhancer Sequence
TTCTAGTTAT TTCTTGATCA TATGCTAAAC AAGGGATAGA TTATTCATGG ATTTTCTGGG 60
AAAGGGGTGG GGAAATCCTG GAATGGAACA GAGGGTTCCT GCCCTTTTTA GACCATGTAG 120
GGTAACTTCT GGCCTTTGCC TGTGGCATTT GTAAACTGTC ACGGGGCTGG TAGGCGTGTC 180
TTTTAGCAGC TAATGCATTA TAATTAGCAA ATAATAAGCA GTGAGGTCGA CCAGAGGTCA 240
CTTTCATTGC CTTCTTGGTT TTGGTGGGTC TTGGCTGGCT TCTTCACCAC ATCCTGTTTT 300
ATCTACGGGG GCTTTGTGAC CTGTGTCTTG TGCCGACCTC CGATCTCATC CTGTGGCTAA 360
GAATGCCTAA CTTCCTGGGG ATGCAGCCCA GCAGGTCTCA GCCTCATTTC CCCCAGCCTG 420
TTTGAGCCGC AGTCGCCCTG GTTCCAATGT CCCTGACAGT AACGGGCACC CCTTTAGCTG 480
CACCCTGCCT TCTTGCCTCA AGGAGGAAGT GCCTGGTCCT GTTCTCTGAG CCGGGTCTCC 540
ACTCGCACTC TGCCGGGGGT TCTCTCCCCT CCTCCAGAGC TGCAAGTGCT GTGGCTGCCC 600
TCTTTCCTGT GCACATCGTC TCTCTTTCAG CAGGCACTGA CCTATCTCAC ATGACAACAC 660
CTTCATTATA TTATACGACG TTATGAGAAA ACCACAAGCC ACTTTCTGGA CCTTATCTAT 720
GTCCTTGTCC AGCTCCTTGT CTCTGCTCCC TTTATGGCAC ATGGATGCAG CAAGGTGGCC 780
TTTATCTCCT GCCTCCTCCT CAACCCTGGC CTTACCACTG AGCTGAGATG GCCATCTCCC 840
CCATCACTGC CATCACGGTG GAGGAGGGGC TCCCTCTTGC TGAAGCCAGC ATCCACCTCT 900
CTGTCCTCTT CTTCCTTGAT GTCTTAGCAG CGCTGGTGTA GACGACTCTC TCCTTCAAAC 960
AGTTTCTTCC TGAAGGCTGC CGGATGCCCT GTCCAGCTGC TTTTCCTTCT ACCTTACTAG 1020
CTGGATTTTT TGTTTTGCTT TGTTTTTAGT TTTCTTTTTG TTTGTTTTTT GAGACAAGGT 1080
CTCCTTCTGT TGTCCAGGCT GGAAGTGCGG TGGAGCAATC TCAGCTCACT GCAGCCTTAA 1140
CCTCCTGGGC TCAGGTGATC CTGCCACCTT AGCCTCCCGA GTAGCTTGGT CTACAGCTAC 1200
CTTTTTTTCC TAAGTACCCT TTGACCATGC CTCTTTCTCT GTCAGATATT TAAATGTCAG 1260
GGTACCCAGA CTGCATGTTC ACTCTTCCAC ATAGACTCGA AAGCAAGCTA ACTCACAGAG 1320
GCAGAGAGCA GAATAGGGGA CTTGAGGCTG GGAGCAGGGC GTGGGGATGT GCTGGTCCAA 1380
GGGTTCAGGG TTTCAGTTAG GCAGGAGGAA TAAATAATGA GCATTTGAGG TGATGGATAT 1440
GTTAGTTAGC TTGTTTCAAT CATTCCACAT 1470