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

TagContent
EnhancerAtlas ID
HS098-22721 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr16:87574520-87575990 
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
CCCTGAGCCT CCCTCAGTCC CCAGATCAGC AGCAGGGATT TTTTTACAGC CCTCTACCCA 60
GCCACCCTGG GTCCTGTGCA GCCAACCTGG GTCCACACAT GTCCGGGACT CACAGATGAG 120
ATGGAACTGT CCCACGCATG GTCTCTGGGG CAGAAACTGC TGCGGAGCCT GCCGAGGCCA 180
CTCCTGCCGA CTGGCCAGGG CACAGCATCT GACCCAGGAG GCTGTGACCT CGCTGCCCCA 240
GGCCTGGCAT GGCCTGTGGA CAGTGGCCCG TCCCGCCGGC CACCAGGAAC CTCCCCTCGG 300
TGCCCACCCC ATCCACCTCG CCAAGACTAA TCTAGAAATT ATTTATAGAT CCGAACTCCA 360
CAGAAACCAT TGTGTCTGCC GTTGCCATGG CAATGGGGAT GTGGCAGGAG CGCCAGGCTC 420
TCAGGCTTTC CAGGGCCCGT GGAGGCCGGC AAGGGCGGTC GATTTCTCCC AGGAGCCCCT 480
GACTCACGCC CACCTTCAGA GGCCCCCGGG AGTGAAGAAG ACAGCCTTCC CACCCGTTTC 540
CAGCAGGGCT GGCTGCATCC AGGAAGACAG CGCTGCTGGT GAGTGGTTCG GCTTTGTTTC 600
AGACCACTCA AAGAAATCAT CTAGAACAAC GTCCGCAAGA CTGGCGGTGC AACTGTCCCC 660
CTTGGAACCT CTCGGGAACA CAGCCTCTGT CTCCTCACCG CAGAGCAGCT GCGTCAGACT 720
CCCAGACGGC GGGGCCTAGG GATCTGTGTT TTGGTTTTGG GATCTGTGCA AATCCACATG 780
ACTCAATAAT CCAAACATAC AGAGAGCCTG GGAACCCTTA CCCCGCTCTG GCGCCCTATG 840
TGTCCGCTTT CATTGGCTTC TTGTATTTCC GGCTTGTTTT CTTTAGGGAG GCAGCAAATA 900
CAAGATACGG TCCACTTTTA TCTTTCCCCG CTCAGAAAAT AAAGATACCA CAGCCCAGGC 960
TTCCGCACCT TGCTTTTCTC ACTAAATACT ATTTTCCAAA GCTGTCACCA AATTCGCCGC 1020
TTCTTTATTT TTTTTTCTTT TACGGCGGCA CAGCATGGGT TCCCTCCTGT GGGTCGGTGT 1080
GCCAAGGAAT CTGCTTGCGT AACCAGACCT TTTCCCTAGG AGCAGTTGCC CAGACGCAGC 1140
CCCTAGGATG AGGATGTGTT TGCAGCGACT ATTCAGGGAG TACTCCCTGG GGACACAGGT 1200
TGGGGGTGGG AAGCTGGACT GGAAAAGGAA GGAAGCTGGG CAGGGTGCTA TGTGGGCACA 1260
GTCCTTCTGC AGCCTGAAGG AACTGGGGTG GGCGGGGCAT GCCCGACCCC ACAGGGGAAC 1320
TGTGGAGGGT CAATCACACC CAGGGATGTC CCAGCCTGAG ACCAGGGAGC TGAGGTCTTC 1380
ATACACCCAC CCAGAACCCA CCTGTCTTTG GTTAAGCGTG GTCTAGGGAG GTATAAATTC 1440
CCAGGCATTT CCGTGCATGA GGGTGAAGCG 1470