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

TagContent
EnhancerAtlas ID
HS062-00210 
Organism
Homo sapiens 
Tissue/cell
GM18486 
Coordinate
chr1:22457810-22459510 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs12404660chr122458794hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr1:22458560-22458579TGGCCTGCAGGGGGCGCCA+7.87
Gata1MA0035.3chr1:22458086-22458097TCCTTATCTGT+6.14
Myod1MA0499.1chr1:22459297-22459310AGCAGCTGTCCCC+7.04
MyogMA0500.1chr1:22459296-22459307CAGCAGCTGTC-6.14
SCRT1MA0743.1chr1:22458544-22458559TCCCACCTGTTGCTC-7.46
SCRT2MA0744.1chr1:22458546-22458559CCACCTGTTGCTC-7.22
Tcf12MA0521.1chr1:22459296-22459307CAGCAGCTGTC-6.02
Number of super-enhancer constituents: 1             
IDCoordinateTissue/cell
SE_65544chr1:22451883-22461737Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12245883522459325
Number: 3             
IDChromosomeStartEnd
GH01I022133chr12245852122458650
GH01I022134chr12245869322458894
GH01I022132chr12245910122459250
Enhancer Sequence
GCATCGAAAC GTGTGCAGGG TTTGTTGAAG GTGGAGGTGC CTGGGCCCCA GTCCCAGTGG 60
GGGTTGGTGG GCCTCTGAGG TTAATTGAAT GTGCCTTAGG TGCACCTGGG AGGCTAGGTG 120
GGCACTGGCC TGGAGAACAG TCTGCATAAG TATGGGTAAT GTTTCCTTCT CAGCCATAGG 180
GAGCTCTGAC TCAGGGATGC CACTGTCCTC CTCACTGTGG CATTGATCCC CAGGATGTTT 240
CCTTTTCCCC GTGGCTGTGG AGCCTGAGCC TGGCTTTCCT TATCTGTAAA TGGAGATAAC 300
GGTTCTCACC CAGAGGGCTG CCAAGAGGAA TGCCCGTGAT TTGCTGTGTG ATGCACCTGG 360
CTGTCAGCTG GGCACATTCT AGGTGCCAGG TAATTGTGGG GGCAAGTGTA CAGCATGGGG 420
CAAGTGCAAA GTAGGCGGTC TCAGGCCGAA GAAGGCCAAC CTCCCCTCCC CACCCCCTGC 480
ATTCCTGGTC TCCCAGGGGC CTCCCCGCCC CTCCTTCCTA TCTACCAGGT GGTTCCCAGG 540
GGATGCACAG ACTGGTGGTG TCCTGACAAG GCCCAGGCAG GAGCTCGGAG CCCCTTGGAG 600
GGAAGACAAG GGCAGGAAGG GGGCTGAGAA GCAGCAGAGG CTGCATTTGG AAGGGGAGGG 660
GCCCACCCGG CTTCTCAGCC CTGCCTGGGT GCTCTCCTGC CTGTGCCCAG CCAAGGGGTC 720
GCCTGTGGAG CCAGTCCCAC CTGTTGCTCT TGGCCTGCAG GGGGCGCCAA GAGCCCGGCT 780
ACTGGCTGTG GGCCAGGTCC ACGTTCAGGC CACAGGTGTC CCTCGGTGGG GGGACAAGGA 840
ATTGAGCCTG ACGTTGGATC CTTTCCTGCT CAGACCGAGG CTTGGCCTCT TGGAGAAGGG 900
TGGGGGCCCT GTTTGCTCTA TGATGTGGGG GCACAGAGCT GGCCCATCCC CAACTCAGTC 960
TCTGCTCCCA CAGCATGCAG CCAAGAAGGC TGCATCTGGC TGTGCTGGGC CCTGGGCTCT 1020
GGTCAAGGGA GGCACCCAAG GGCAGGGGTT CTCTGGGCAG GGGGGGCAGC CTCTGACCCA 1080
CCATGACCTT GGGCAAGTCC CTGCCATACT TGGAGCCTGT CTCCTTATGG GTACAGTAAA 1140
CCGGTGGGTC CATATGGCCT TTCCCACTGT CGGAGTTGGT GGGCCTCCTT CTACTGGCAG 1200
GGTGGGGAGT GGCCGGGCCT CAGGGGCCTG CTGGCCCCAT GCCAGGCTGA TAGATGTGTC 1260
TCTGCCATTG AATAAGTAGT AAGATGGACC AGGGGAGCCA CCTGCATCCC CCCACCCAGG 1320
CTCAGAACTC AGCAAGGGGA GACTGGCTGA ATGACAGTCG CAGGGGCTTA GGGTGAGCTG 1380
CTGGGCTGCC GTGGCCGTGA GTCACTGGGC CAGCTTCCAG GAAGGAGCTG AGCAACCTCT 1440
TCCGTTGGCA CCAGTGCCCA CCCCCAGCCC CTGCCTTCAT CTGGCACAGC AGCTGTCCCC 1500
TTCCGTACAC ACGAGGCCCA GCCCCATCCC CACCCCTGTT CCCCCAGACC CCAGGGTCTC 1560
GCCCGGGCAG GGCTGGGTGC CAGGGCTGGA AATGGAACCG GGCACCGGCT CTAGAGAGTG 1620
AGAACCCCAG GCATTACAGG CCCTCATCCA CAATGTTTCT GCTTGCCCGT TTCAGTATCC 1680
AACTAGCATT TGGCTCCATT 1700