EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS118-07640 
Organism
Homo sapiens 
Tissue/cell
Liver 
Coordinate
chr16:87573760-87576200 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs12445022chr1687575332hg19
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RFX1MA0509.2chr16:87574899-87574915CGTTGCCATGGCAATG+6.44
RFX1MA0509.2chr16:87574899-87574915CGTTGCCATGGCAATG-6.47
RFX2MA0600.2chr16:87574899-87574915CGTTGCCATGGCAATG-6.99
RFX2MA0600.2chr16:87574899-87574915CGTTGCCATGGCAATG+7.04
RFX5MA0510.2chr16:87574899-87574915CGTTGCCATGGCAATG+7.24
RFX5MA0510.2chr16:87574899-87574915CGTTGCCATGGCAATG-7.27
SP2MA0516.2chr16:87575805-87575822GGGTGGGCGGGGCATGC-6.15
SP3MA0746.2chr16:87575806-87575819GGTGGGCGGGGCA-6.05
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr168757480387575451
chr168757485187574952
Number: 1             
IDChromosomeStartEnd
GH16I087540chr168757395187575870
Enhancer Sequence
CTGCCACTTC CAGCCCTTCT TATTTCTCTT GAAAGCTGTT CTGTGTCCAC ATGGATGGAG 60
CCACCACGCT TTTTGCTGAC TGCACAAGAG CTCTCAGTGC ATGGGGAGTA GGCTGTCCTT 120
CTCCACTCCT CTCCACCAAC AGGCATGAGG CTGCTCTCAG TCTCTGCTGT AATCAACGCA 180
TGGCGTGGGT CATGCCTTTG GCACATATAT GCCTTTGTGC CCCTATGCCA GTGCCTCACT 240
CAGGAAGAAT CCTCGGAGGA GAACTGCTGC GCAAGAGGAT TTGCCGTTGT CAGTGCCGGG 300
GCTGTGGTTA AATTGCCTCC CCGTAGGCTG CACTTGCTCA CACGCCTGCC CTCCCGGTGT 360
CAGGGTCATG CCCCTCACTC CTAACGCCAT GCAGCACGTA GCCATTCAGG GGCCCTTTGG 420
GGGCCCCTCC CAGCGAGCTC ACTCTAATCA GAGACAGCAA AGGTGTTGGA TCTGCTTGAT 480
TTTCAAATGA TTTACCCAGA AGCATCCACC CTCTCAGCCC CTAGTGTGGG GAATATGAGC 540
CCTTCCCTGG AAACACTGCT AGAAAAAGAA AAAAAAAAAA AGGAAGAGAG AGAGAGGGCT 600
CATTGAATAG GGCATCCCTA AAACGTGGAC AGAGGAAGCA GAGAGAATGG AGTCCAAACA 660
CTCAGATCCT GTTGTCACCC CACCAGGGTC TACCCAGCAA CGCCGAGACA CTGAACAGGG 720
CCCTCGTGAG TGCCTAGAAA CGGTGGTGAT CAACTCCCAC CCCTGAGCCT CCCTCAGTCC 780
CCAGATCAGC AGCAGGGATT TTTTTACAGC CCTCTACCCA GCCACCCTGG GTCCTGTGCA 840
GCCAACCTGG GTCCACACAT GTCCGGGACT CACAGATGAG ATGGAACTGT CCCACGCATG 900
GTCTCTGGGG CAGAAACTGC TGCGGAGCCT GCCGAGGCCA CTCCTGCCGA CTGGCCAGGG 960
CACAGCATCT GACCCAGGAG GCTGTGACCT CGCTGCCCCA GGCCTGGCAT GGCCTGTGGA 1020
CAGTGGCCCG TCCCGCCGGC CACCAGGAAC CTCCCCTCGG TGCCCACCCC ATCCACCTCG 1080
CCAAGACTAA TCTAGAAATT ATTTATAGAT CCGAACTCCA CAGAAACCAT TGTGTCTGCC 1140
GTTGCCATGG CAATGGGGAT GTGGCAGGAG CGCCAGGCTC TCAGGCTTTC CAGGGCCCGT 1200
GGAGGCCGGC AAGGGCGGTC GATTTCTCCC AGGAGCCCCT GACTCACGCC CACCTTCAGA 1260
GGCCCCCGGG AGTGAAGAAG ACAGCCTTCC CACCCGTTTC CAGCAGGGCT GGCTGCATCC 1320
AGGAAGACAG CGCTGCTGGT GAGTGGTTCG GCTTTGTTTC AGACCACTCA AAGAAATCAT 1380
CTAGAACAAC GTCCGCAAGA CTGGCGGTGC AACTGTCCCC CTTGGAACCT CTCGGGAACA 1440
CAGCCTCTGT CTCCTCACCG CAGAGCAGCT GCGTCAGACT CCCAGACGGC GGGGCCTAGG 1500
GATCTGTGTT TTGGTTTTGG GATCTGTGCA AATCCACATG ACTCAATAAT CCAAACATAC 1560
AGAGAGCCTG GGAACCCTTA CCCCGCTCTG GCGCCCTATG TGTCCGCTTT CATTGGCTTC 1620
TTGTATTTCC GGCTTGTTTT CTTTAGGGAG GCAGCAAATA CAAGATACGG TCCACTTTTA 1680
TCTTTCCCCG CTCAGAAAAT AAAGATACCA CAGCCCAGGC TTCCGCACCT TGCTTTTCTC 1740
ACTAAATACT ATTTTCCAAA GCTGTCACCA AATTCGCCGC TTCTTTATTT TTTTTTCTTT 1800
TACGGCGGCA CAGCATGGGT TCCCTCCTGT GGGTCGGTGT GCCAAGGAAT CTGCTTGCGT 1860
AACCAGACCT TTTCCCTAGG AGCAGTTGCC CAGACGCAGC CCCTAGGATG AGGATGTGTT 1920
TGCAGCGACT ATTCAGGGAG TACTCCCTGG GGACACAGGT TGGGGGTGGG AAGCTGGACT 1980
GGAAAAGGAA GGAAGCTGGG CAGGGTGCTA TGTGGGCACA GTCCTTCTGC AGCCTGAAGG 2040
AACTGGGGTG GGCGGGGCAT GCCCGACCCC ACAGGGGAAC TGTGGAGGGT CAATCACACC 2100
CAGGGATGTC CCAGCCTGAG ACCAGGGAGC TGAGGTCTTC ATACACCCAC CCAGAACCCA 2160
CCTGTCTTTG GTTAAGCGTG GTCTAGGGAG GTATAAATTC CCAGGCATTT CCGTGCATGA 2220
GGGTGAAGCG GCTTCAGAGA GCCCACAGGC CACCCTCTAA ACCAGAGGTC TCCAACCCCC 2280
GGGCCACGGC AGAAGGTGAG CAGCAGGTGA GTGAGCAAAG CTTCACCTGT ATTTACAGCT 2340
GCTGCCCACG GCTCACGTTA ACACCTGAGA TCCGCCTCCT GTCAGATCAG CCGCAGCATT 2400
AGATTCTCAT AGAAGCGTGG ACCGTATCGT GAGCTGCATA 2440