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

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EnhancerAtlas ID
HS180-16354 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr15:52579820-52581600 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs113338370chr1552580536hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF4MA0039.3chr15:52580658-52580669CCACACCCTGC+6.62
ZNF143MA0088.2chr15:52580802-52580818TACCCACAAAGCAATG+6.31
ZNF263MA0528.1chr15:52581320-52581341CTCTCTTCCTCCTCCTCTTCA-6.3
ZNF263MA0528.1chr15:52581323-52581344TCTTCCTCCTCCTCTTCATTC-7.01
ZNF263MA0528.1chr15:52581317-52581338CCCCTCTCTTCCTCCTCCTCT-8.17
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr155258053052580869
chr155258114052581245
Number: 1             
IDChromosomeStartEnd
GH15I052286chr155257918052582470
Enhancer Sequence
ATTATCTACT CCAAGTTGTT TGTCAAACTC CTTTTTAGAG CTGCAGAAAG CCTACTTCAA 60
AAGGAAGTTC TGGCCAGGCG CGGTGGCTCA CGTGTGTAAT CCCAGCACTT TGGGAGGCCG 120
AGGTGGGTGG ATCACCTGAG ATTGGGAGAT TGAGAATAGC CTGACCAACA TGGAGAAACC 180
CCGTCTCTAC TAAAAATACA AAAGTAGCTG GGCGTGGTGG CGCATGCCTC TAACCCCAGC 240
TACTTGGGAG GCTGAGGCAG GAGAATCGCT TGAACCCGAG AGGCGGAGGT TTCTGTGAGG 300
CAAGATCTTG CCATTGCACT GCAGCCTGGG TGACATGCGT GAAACTCCGT CTCAAAAAAA 360
AAAAAAAATT AAGTTGTAAC AGCTGGCTAA GCGAAGCTGG TGAAAGTGGA GGTGTTCTGA 420
TGGGAGCTGG AGCTGAGAGC CCTGGGGGCC TTCCAAGGAA GCCTGGGCTC TGAGAAGTAA 480
TGTGAAAGTC ACTAGGCCAA TCAATCCTTT TGTTTAACAG AGCCCCTAAC TGAAGCCCAG 540
AGAGAAATAA CTCACCAAAC AGCAGACAGA GTCTCAAAGG ACCAGGACTC CAGCAGAGCT 600
AGGGCCTGTG ACTCCTAGTT TGAACTCCGT ATTAGTTAAG CGAATCTGGC CCTGAAAGTA 660
ATCCTGAACT CTGAACTGCA ACCATCTACT TGAGAGTCCA TGTGCTCTCC TAACTATAAT 720
TTAGGATTGG TTTCAGCTAA AAGTGGTATT AAATGGCAGG CAGTATTAGG ACATACGTAA 780
CCACTGACGG CTTCTCTTCT GAAGACCAGT GACTCCTCAG CCCAGTACCC CAGGCCGCCC 840
ACACCCTGCG ATCCTGGTGC TTCTGCTGGC ATTGAGTGCC CTGCAGCTGA AACCCAGCCT 900
GGTAAGTAAA CAACGGTGAG TTTACTCAGC TCCGGGTAAG TTCCACCCAT TCATTCCTGT 960
CCCCTCCTCC CTCACATTCC TCTACCCACA AAGCAATGCT TCAAACTGGA GGAAGAGTTA 1020
ACTTTACAGC ATTCATCCAA ACAGATGCAG TCCGCAGTTC ATGCAAACAA TGTAACCAGC 1080
TGTCAACTGA CCTCCAGAAT ATGGGGCCTT CCCATGAGGC AGGAGTCTGT GGACTGGGAT 1140
GGAACAGCTC GCCAAGCCCT TCAGCGGAGC CAGGAAAGAG AGGGCCACCT CCCAACTTCC 1200
CTGAGTGCCC TCCCCATGCC AAGGCGCCAA GCTGAGGCAG AGGCTCGGGA CCACTGAACC 1260
TTATGAGCTC AAGACCATGC CAGCCACCCC CCCAAGGCAC ACAGGTGAGA TGAGAACAGC 1320
ATCTTCTCAC GCCGCCTGCT TTTCTGAGGG ATCTTCTGGC ATGAGCCACA GAAATGACTT 1380
GAAGACTTAT ATGGAAGATG GGACAAGATG GGACGACATG TGTTTCCCTC CTAGAACCGC 1440
TTTCTGGACT GGGAGTGTCC ACACTCCAGG TCAGCCAGGC CAGATTGTCA CACCATGCCC 1500
CTCTCTTCCT CCTCCTCTTC ATTCGCTCCT CATGGGCCCC TCCCCTGGCT CCCCTGCCCC 1560
TCCCACTGCC CCCCATGTCC GTGTCTCCCA AGGTCCTTCC CAGCCTCTTC TCATGATAGG 1620
CTGTTTCTGG AGAGTTCCAC CCAATTCCAC AGCTTCTGCA ACTGCCTGGC ACCTGTGCAT 1680
CTGAGACCTC CCACCCAGAT CGTGCACTGG AGCTCTACAC CACATTTCCA ATTGCCTCCA 1740
AGATGTCAGC CCCTAAATGT CCTCATAGAC TCATAAATTC 1780