EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS064-02682 
Organism
Homo sapiens 
Tissue/cell
GM18507 
Coordinate
chr11:73034820-73037640 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs2027761chr1173036179hg19
rs2027760chr1173036481hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF5MA0599.1chr11:73036844-73036854GGGGCGGGGC-6.02
Nr2f6(var.2)MA0728.1chr11:73037548-73037563GAGGTCAGGAGTTCA+6.22
RREB1MA0073.1chr11:73036254-73036274GCCCAAACCTCCCCCACCCC+6.39
ZNF263MA0528.1chr11:73035002-73035023TCCTTCTCCCTGTTCTCCTCC-7.07
ZNF263MA0528.1chr11:73034824-73034845GGTGGAGGAATAGGAGAAGGG+7.19
Number of super-enhancer constituents: 26             
IDCoordinateTissue/cell
SE_01582chr11:73030301-73037752Aorta
SE_02882chr11:73031862-73036852Astrocytes
SE_04339chr11:73031975-73037551Brain_Anterior_Caudate
SE_06140chr11:73030318-73037316Brain_Hippocampus_Middle
SE_26016chr11:73031691-73037258Duodenum_Smooth_Muscle
SE_27041chr11:73031604-73037579Esophagus
SE_30618chr11:73031986-73036224Fetal_Muscle
SE_32060chr11:73031782-73037392Gastric
SE_39001chr11:73031680-73037276IMR90
SE_40817chr11:73031658-73040101Left_Ventricle
SE_42282chr11:73031638-73037644Lung
SE_44364chr11:73031680-73037150NHDF-Ad
SE_44992chr11:73031717-73036952NHLF
SE_45900chr11:73031646-73037694Osteoblasts
SE_46937chr11:73034753-73035669Ovary
SE_46937chr11:73035818-73036170Ovary
SE_46937chr11:73036224-73036621Ovary
SE_48721chr11:73031870-73037646Right_Atrium
SE_49552chr11:73034776-73036223Right_Ventricle
SE_50607chr11:73031699-73037502Sigmoid_Colon
SE_53958chr11:73031625-73037049Spleen
SE_53958chr11:73037078-73037621Spleen
SE_54638chr11:73017438-73040151Stomach_Smooth_Muscle
SE_60317chr11:73022596-73047103Ly4
SE_65783chr11:73032656-73036525Pancreatic_islets
SE_68363chr11:73017636-73046660TC32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr117303611773037003
Number: 1             
IDChromosomeStartEnd
GH11I073319chr117303058473039310
Enhancer Sequence
GGCTGGTGGA GGAATAGGAG AAGGGTGGGC CCGGCCTGCC CCATCTCATC ACCTGGACGT 60
GGTGCCTGGG CAGTGGAGGG TCTCTGCTGG TCCCCTGGGC ATCTGTGTCT TTGTTCCAGC 120
CACTCGCACC AGGACTTCCT CTCATGGAGG CTCCCTGCTT TCTTCTCTCC TTCTGTCCTC 180
TGTCCTTCTC CCTGTTCTCC TCCCTGGGTC TTGCTCCTCT TCCTGTCTCT CATCTCCTCT 240
GACCATCTGT GTCACCCTGC CTCCCTTTAG AGAGCCAGAC AGAGACCCCT GGCCAGGGAC 300
TGGTCTTAGG AAAACGGCCG TGTAGGGCAG AGTCCCCCTC AGCTTCCCAG CCCAGGTGTC 360
AGGAACCGCC TCTGTCCCAG GATACACAGT GATTGCAGCT CCTCTCTGCT TCGGAGGTAA 420
CAGACCTCTA AGGCTCTGGG ATGTGGAGAT GTGGGTGGGA GCCCCCAGTT TGCCCCGTGA 480
CCCAATGCTT GATTCTGGTC GGGTGGATCC ACCCATGCCA AGCCCTCCTG TTCCTGGCAC 540
GAGGTGGAGC CTGGGTACAC GTTTATTAAA TAAATAATGT GGGGGAGGCA GGAGGAGGAC 600
AGCTGAGCCC TGCCCTGGGG GAGCGCCCAG GCTCCTCTCA GCTCCCCTTA CCACCCATGC 660
CTATGCCTAG CCCTATGTTG CTGCTGTCCT GGGGACCAGG CAGGTGGAAG CTGGCAGATG 720
GGCAAAGGGT GCCGTCCCGA GTCGGCACTG ATTGGGGGTG GGATGGGAAG CAGACACAGG 780
CCCAGAGAAG GTGAGGGTGC TTAGCTCAGG TCACAGAGCC CAGAAAGAGA GAGGTGGTAT 840
TCAAACCAGG ATAGTCTCAC TGGGTTGGAG TTCAGACCCA GATGGTCTGG CTCCAGAACC 900
CGTGCTTAGG CCCCTGGCTT TCAGGACTGC CTGAGTTGGG GGCAGTGCCA TCATCAAGGT 960
GGGCACAGAA AGAAAGGGTG GATTTTGCTT TGGACATAGT GATCCTACTG GATTCACAGT 1020
CCATGGTCTG AGTCCCAGGA ACCAGCACAT AGTAGTTGCT CAGTAAATAT TAGTTGAATG 1080
GCTCAGTTGC ACTTGAGAGG CCCTTGGGGA GTGGGAGGAG GTGACAGGCA CAGAAGGAAT 1140
GAGTGTTTCC TCCCTTTATG GGCCCAGGGA CCCTTCTCTT GGTGCTGGAA AGCAGCTGAG 1200
GTGGGTGCTG GGCTTTCTGC TGGCGGAGAG AACTCAGCCC AGGAGTTTGG GAAGGTGGAG 1260
AGATGGGCCA CGGGCAGGTG AAGGGGAGAC AGGCAGGCCA GGCAGTGCAG TGCAGTCCCG 1320
TTTGCAGTAT CTGGAAAGCA GATCTCTTGG GCCATGGCCG GCGTGACTCA AATGGAGACA 1380
AAAAAACCTT CCATATTTGG ACAAAGAGCC CAGAGAGGCC CAGACCCGCA GCCAGCCCAA 1440
ACCTCCCCCA CCCCCAGCCT CCTGCCCTGT CTCCCTCTGG GCCCCTAGCC CTGAGTCCTG 1500
TCCCATGAGT TGAACTCTTG GGCCTCAGTC ATCAGGTCGC TTCCTGTGTG GCCAGGCCTG 1560
GGCTGTGGGT GCTGGGGAAG AAATTTCGTT CCAGGGCTGG GCCCTGTGCT TGGGCTGGAG 1620
ATGTAGAGAG GAGCCCTGCT GGAGCCTGCG GGCTGGAGGG GAGCACACTG AAACCAACAG 1680
TTCCCACACT GTGGGGTAAG CTGACAGCAA ACCCCCACCC ATCTCAACAC AGGCAAAGCT 1740
TGAGGAGCAT CGCATATAGG CATTGTACAC ACACACTCTC TCTCTCTCTC TCACTTTCTC 1800
ACTTTTCAAT CCCCAGCAGA TTTCCATACC CACAAAGACA TCTGTACAGA TATCAGGAGT 1860
GAGGACCGAG CCTGAGACCT TCCCTGGAGC AAGCTTTGAT GACAGCAAAG TTGGAGTAGA 1920
TTGGGGCAGC CAGATGTCAA CAAGTAACAT AAACAGGCAT TATCCATCTG GAGAGATGTG 1980
AACAGAGCAA TTTGCTCCTG TACCACCCTC TGAGTGTCCA GCAAGGGGCG GGGCTGGGCA 2040
GTGGATGCCA GAGCCTGGTG AGTGGGGAGA GGGCCTAGGC CGCTTCCTGC CTGGGAGCAG 2100
ACCTTGCTCC CATGGGACAG CCCAGCCATT TGACTGAGAA CCGGGGTGTT CACTGTCATT 2160
GGTGGATTGA CTGAGCCCTG ACTGCACAGA TGCTTCTACC TTTTCTAACT AGTCTTGGAT 2220
AATTAACGCT GAAATAAGCT CTGAGTGGCG GGTTGGGGGA ACCCAGGGGA ACCTTTAAAA 2280
TTCAATTGCA CTGTGGCCCA CTGGTGCCTG TATGTGCAGG GTTAGCATGG GGGCCGCAGG 2340
GTGAAGGAGA AGGGGTTCCT GACCCAAGAA GCCCCATCTG AGAACTGGGG GTCGAAGGAG 2400
GCCAAGAAGG GTGAGGGCAG GGAAGGCTAA CTTAGGGCAG TGGCTGGAAT CTTGAAGGAC 2460
TAGCCAGACC TTGACAGGCA GAAATGAGCC AAGGCCCTTC AGGGAGAGAG AACTGCAAAG 2520
GTAGAGGCCT GTGATGGAGA AGCCCTGGTG TGTCTGGGGT ACCATGAAAG CTCCCTGGTT 2580
CTGGAGAGGT CAGGTGGGCC CCGGGAGTTC CTAAAGGCCA GGCCTAAAAG CCTGGACTTG 2640
ATCCCAGAGT GGTAATTTCC AAGCTCACGG CTGTAATCCC AGCACTTTGG GAGGCCGAGG 2700
TTGGGAGGCC GAGGAGGGCG GATCACCTGA GGTCAGGAGT TCAAGACCAG CCTGGTCAAC 2760
ATGGTAAAAC CACATCTCTA CTAGAAATAC AAAAATTAGC TGGGCCTGGT GGCATACGCC 2820