EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS049-05326 
Organism
Homo sapiens 
Tissue/cell
Fetal_spinal_cord 
Coordinate
chr22:37724280-37727510 
TF binding sites/motifs
Number: 22             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RFX1MA0509.2chr22:37726672-37726688GGTCGCCATGGAAACC+6.14
RFX1MA0509.2chr22:37726672-37726688GGTCGCCATGGAAACC-6.16
RFX2MA0600.2chr22:37726672-37726688GGTCGCCATGGAAACC+6.47
RFX2MA0600.2chr22:37726672-37726688GGTCGCCATGGAAACC-6.57
RFX5MA0510.2chr22:37726672-37726688GGTCGCCATGGAAACC+6.15
RFX5MA0510.2chr22:37726672-37726688GGTCGCCATGGAAACC-6.25
ZEB1MA0103.3chr22:37727251-37727262CCCACCTGCCC+6.14
ZNF263MA0528.1chr22:37725198-37725219CTCTCTCTCTCCCCCTCACCC-6.14
ZNF263MA0528.1chr22:37724955-37724976TCTCCCTCTCTCTCTTCCCCT-6.18
ZNF263MA0528.1chr22:37724486-37724507CCTCCCTGTTTCTCCTCCTTA-6.25
ZNF263MA0528.1chr22:37727075-37727096TCTCCTTCCCCCTCCTCCCTG-6.2
ZNF263MA0528.1chr22:37724990-37725011CCCTCTCTCTCTCTCTCCCTC-6.32
ZNF263MA0528.1chr22:37725054-37725075CTCTCCCTCTCTCTCTCCCTC-6.34
ZNF263MA0528.1chr22:37725102-37725123CTCTCCCTCTCTCTCTCCCTC-6.34
ZNF263MA0528.1chr22:37725192-37725213CTCTCTCTCTCTCTCTCCCCC-6.3
ZNF263MA0528.1chr22:37724483-37724504CCCCCTCCCTGTTTCTCCTCC-6.77
ZNF263MA0528.1chr22:37725745-37725766GGAAGAGGGAGAGAAAGAAGA+6.81
ZNF263MA0528.1chr22:37725739-37725760GAAGAAGGAAGAGGGAGAGAA+7.01
ZNF263MA0528.1chr22:37725073-37725094TCTCTCTCTCTCTCCTCCTCT-7.26
ZNF263MA0528.1chr22:37725742-37725763GAAGGAAGAGGGAGAGAAAGA+7.36
ZNF263MA0528.1chr22:37725070-37725091CCCTCTCTCTCTCTCTCCTCC-7.52
ZNF263MA0528.1chr22:37727072-37727093CCATCTCCTTCCCCCTCCTCC-7.54
Number of super-enhancer constituents: 4             
IDCoordinateTissue/cell
SE_34245chr22:37710962-37729737HCT-116
SE_55695chr22:37724192-37727925u87
SE_61487chr22:37701837-37826067Toledo
SE_67720chr22:37724192-37727925u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr223772732837727420
Number: 1             
IDChromosomeStartEnd
GH22I037325chr223772193537729260
Enhancer Sequence
TATAGCTGGG ATCATCTCCC TCCCTGGCTC AACAACTTTC AGATGCTTCC CAGGTTCTCT 60
CTGTCAAGGC CCAGCCTGGT CTTCAAGTCT TGAAGCCCTA TATGAAATGG CTCTGGTTCA 120
CCCCCGCAAC CTTGTCTCAA GCTGCATCTC CCATACAGTC TTCCCGAAGC AGTCCTGGCC 180
TCCAAGCCTC CATTCATGCA GTTCCCCCTC CCTGTTTCTC CTCCTTAGCC TACCCACATT 240
TGTGCCTGTG GGGGCCCTGG CCATCCTTGG AGATCTTACA GGGCTTCAGC AATCCAGGGG 300
CACCTGCAGT AGGGACCAGC TACCCCATTT CCCAAATCCC ACAGCAGAAG GCAGTGAGCA 360
GGGGCTTTGA CCAGGAGGAC CTGGGTCCCA AATGAATCCT GCCAATGTTT ACTATGGAGA 420
TGTCAATTCG GCTCTTGGAG TAAAGAGGAA GAGTCCCTTT TACTTGTCTC CTGGGGCTGC 480
TGTGAGGTTA GAGATACTGT AACCTCTCTA GCGCACAGTA GGTACTCAAT AATGGACAGC 540
TATTTCCAGC CTGTACACAA CACTTCTGTC CTTCTGAGAG GAGGCTCAGA GAGCAGACCT 600
ACAGCTCCCC GCAACCTGCA GCCCCAACCT CTCTCTCTCT CTCCCTCTTT CTCTCTCTCT 660
CCCTCTCTCT CTCTCTCTCC CTCTCTCTCT TCCCCTCTCT CTCTCTCTCT CCCTCTCTCT 720
CTCTCTCCCT CTCTCTCTCT CTCTCTCTCT CCCTCTCTCT CTCTCCCTCT CTCTCTCTCC 780
CTCTCTCTCT CCCTCTCTCT CTCTCTCCTC CTCTCTCTCT CTCTCTCCCT CTCTCTCTCC 840
CTCTCTCTCT CTCTCTCTCT CTCTCTCTCT CTCCCTCTCT CTCTCTCTCT CTCCCTCTCT 900
CTCTCTCTCT CCCTCTCTCT CTCTCTCTCC CCCTCACCCC CGACAGTGCC TGCAGCCACC 960
GACTGATGCT GGCGTGGACA GAATGACAAT GAGGCCAGGA CCTAAGCGAG CCCATCTGGG 1020
AACCTAAGAC TGTGGCAGAG GCTCAGATGA AGCCAGGGCT TGGGAGGGGC TAGACAGGGA 1080
CGGGGCAGGC AGGCAGGGCA GAGCAGGGAT AGGAGCAGGG CAGTGATCTG CCACTGACTG 1140
TACAGCTGGG TGTCAGCTTT CCCTTCTGCC CAATGGGTGA ATCATTCCCC CTCTCAGGTC 1200
TTGTCCTGAG TACCAAGGGC CAAGTGAGAG TTTGGGATGA AGAGGGACAG AGCCAGGCAG 1260
GGCAGGAGCC AGGGAGCAGG GCAGCGGCAG GGTGGGACCA GGGGATGGGG TTCACGATGG 1320
AGATGGGGCT GGGGCAGGGA CCAGTCAGAT TTCTGATTCA GAGCAATTCA GATTGCTTGG 1380
GCAATCAATC GGACAAAATC ACCCCCAGGG CAGGAAAAGA GACAGTGAGA ATATTGTTGG 1440
AGGGGGTGGT GCGTGCAGGG AAGAAGGAAG AGGGAGAGAA AGAAGAAAGA AGGAATCTGA 1500
GAAGAGACCG TGGAGGGGAC GGGGAGAAAC CATCCCCTGC TGGAGTCCTG GAGGCAGCCC 1560
CACTGGTGCC AGCCTTCTCC TTTGGCCGGT GGGACCTCTG TGGCCAGAGG GCCAGGGACT 1620
CACCCAGGCC CCAGTGAGGG GGAGGCAGAA TGGACAGAAT AGGTGGGAAG ACGGGCATGG 1680
GAAAGGGGTA AAAGGGGAGG TAGGGTGTGG TTGGCACAGG CCTGCATAGC TAACAATCAG 1740
AGAGACGGCC GCCCCTCCTT TTCGAGTCCA CATCACAGGT GGAGGGGCCA ACTCTTGCCA 1800
CACGGCCAGC TCATTCCACC TCATTGCCTT TGCCCAAGCC AGTGCCCTGC CTGGGGTGCC 1860
TTTATTTCCC TACCCTCACC CCAAACATTT AATCCTCCTC CCTAATTCCT CCAACATTCA 1920
CCCCAGCCCT GATCTCCCTC AGCAATGACT GTCTCACCCT CACCCTCAGA GCTTGGTGTG 1980
AGCGGGGTTA CAGTCTGGTG GTCCAAGGAT GCTTGCTGGT GTCCCATAAA TGTGCTTAGT 2040
CCTCACAAGC AGCATGGACG AGCATCACAG CCTGGTGGTT AGGCTCACAG GCTTGGGACT 2100
CCACTGGGCC AGGTTCTAGT CCCAGCAGCT TCGTTTTCAC ATAGTAGTTG CTTCATAAAT 2160
GCTAGGTCCC CTCCTCCTGT TCCATTGCTA GCTCAGAATG TGCACACAGC AGGTGCCCAG 2220
TGGTGGCTTC TGGGCTGAGG TGCCCTTCTG TTCCCTAGTG GGCCCCTTGT CCCTGACAGG 2280
ACACAAAGAT GTCACCCCTG CCTTGGCCTC CAGGCCCAAG CCTGAGCAGT GAAGCTTGGG 2340
AGAAAGGCCC CATTGCTCAT TCCCCTTGAG TCTGCAGCTT GGGCAATCAA TCGGTCGCCA 2400
TGGAAACCAG CCTTCCAATC AGAAGCAGGC ACTTCTTGGC TGCGCCAGCG CCACCTACCC 2460
ACCCACTCAG GCCTGGCTGT GCGGTCCCTC ACCTAGGACT GCCAGGGGTT GGGGGCGGGG 2520
AGGAGAAAAG GGAAACTGGC ATAATTGGGG CACACCTGCT TCTATCCCTA AAGCCCTGAG 2580
AGTCTCCAAA GAAAGAGCAT TTTCTTGGGG TGGGGGTCAC TACTTCAGTG GCCCCCTGAT 2640
TTTTACAGCA TTCATTCCTA CAGAGTATGG CCCTTGGTAC TCAGAACAAA ACCTGAGGGG 2700
AGGGAATGAT TCACCCATTG GGCAGAAGGG AAAGCTGAGA CCCAGCTGTA GGGTCAGTGG 2760
CAAAGCTAGG TGCATGCCCC CTCCCTGAGC CCCCATCTCC TTCCCCCTCC TCCCTGGCCT 2820
GAGGAATGGG ACAGGGAAAG GAGGGGCAGA AGAGTTCCTG GCCCACTGCA GCCAGCACCT 2880
GCCTTCCCAC TAAATCTACG CCTGGCACTT CCAGGGCCCA TTAGCGCCGG GCCCACCAGG 2940
GCCCATTAGC CAGCATCTAT GGGCCTCTGC ACCCACCTGC CCACCCACGC CCAGCTGCAG 3000
CCTCCCGCCC AGGCCCCTCC TTCCCCCACT GCCAGCTGGG ATTGGACAGA GCCCAGGCTC 3060
TGAGTCACAC AACCCCACGT TCAACAACTG GCTCCTCGCT GCTGAGACTA AGCAAGCCAG 3120
GAAACCTCTC TGAGCCTCAG TTTCTCTGTT TGGAAAATGG AAAGAATTAC TCCTGCCTTA 3180
CAAGGGAGTG ATGAGGACTC AGAGTGCATA AAGAGCTTAA CACAGGGCCT 3230