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

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EnhancerAtlas ID
HS062-14667 
Organism
Homo sapiens 
Tissue/cell
GM18486 
Coordinate
chr6:170838450-170839630 
TF binding sites/motifs
Number: 11             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr6:170839089-170839108CACTGCCATCTGGCGGCCT-6.02
RREB1MA0073.1chr6:170838766-170838786CCCCCACCCACCCACCTCCC+8.06
ZNF263MA0528.1chr6:170838750-170838771CTCCCCCTTTCCCTCTCCCCC-6.37
ZNF263MA0528.1chr6:170838736-170838757CTCTCTCTCTCTCTCTCCCCC-6.3
ZNF263MA0528.1chr6:170838693-170838714TCCTCCTCCTTCTTCTTCTTT-6
ZNF263MA0528.1chr6:170838675-170838696TGCTCCCTTCTCTCCTCCTCC-7.1
ZNF263MA0528.1chr6:170838690-170838711TCCTCCTCCTCCTTCTTCTTC-7.39
ZNF263MA0528.1chr6:170838678-170838699TCCCTTCTCTCCTCCTCCTCC-8.32
ZNF263MA0528.1chr6:170838687-170838708TCCTCCTCCTCCTCCTTCTTC-8.69
ZNF263MA0528.1chr6:170838681-170838702CTTCTCTCCTCCTCCTCCTCC-8.79
ZNF263MA0528.1chr6:170838684-170838705CTCTCCTCCTCCTCCTCCTTC-9.89
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr6170838858170839485
Number: 1             
IDChromosomeStartEnd
GH06I170529chr6170838453170839236
Enhancer Sequence
AGAGAGAGAG AGAGAAGCAG AAAAACTAAA CACTGAAACC CAGAGAGAGA GAGAGAAGTA 60
GAAAAACTAA ACACTGAGTC TTAATCTGTT CTGCCACTAG TCAGCAGCCT GCACAGAGCA 120
CTTTAATGTA TTCTCTGTCC ATTAGTTTCC TTGTTTATGA AAGTATATAG CTCCAAAAAA 180
ATTCTGTGTT CTGATTTTTG TCTCTCCAAA CCACAACCAG TCCCCTGCTC CCTTCTCTCC 240
TCCTCCTCCT CCTTCTTCTT CTTTCTCTCT CTCTCCCTGT CTCTCTCTCT CTCTCTCTCT 300
CTCCCCCTTT CCCTCTCCCC CACCCACCCA CCTCCCAACC CCTGCATACA CCTAGGACAC 360
CTCCAGCATA GGTTACTACC AATTTTGCAC ACCTCCAGCA TAGGTTACTA CCAATTTTGC 420
TGGGTTTATC TCCTTCTGTC CTTTCCGCTT TGATCTGAGG AATAGCTGAG ATTTAGGACA 480
GCAACAAGGT GTACCTCCTT CCAGGTTATA AAACAGGATT AATGATTAGG CTCAAGGCCC 540
CTTCCTAGTC ACTCAGTAAA GTCTGTGCAC TGGAAAACTG TGGTAGCAGT TTTCTGAGCA 600
TTAGAAAACT GTGGTTCTCA CAGAGGCTGG ATGAGTCAAC ACTGCCATCT GGCGGCCTCT 660
TGGAGGGTGA TGTGGAGCCT GGCTTTCATT GAAGAATGAA GGTCCCTTGA TTTCCTGACC 720
CTCAGCCAAC TCTCCAGCAG CTTCTCACTG CAGAAGAGGT CAGGCCATTG GTCAGCTTGA 780
GGACAAAGTG GGAGGATCAC ACTTTCGATC ACCTATACTT TCTAACAATC AGCCCTGTGG 840
ACATCTGCTC ACGCCCCATG CTGTTTTTAA AATATTTTCC CATTATAGAA ATATTTTTCA 900
AAGATGATTC ACAAGCTCCA GGAGCCATTC AGACAAGGGA GAGCAAATTG GCAGCTAAAC 960
TCATTCAAGA GTGGAGCAGA TGCACATGAA GCTCTGTCTG GCGGAGGAGG CACAAGACAC 1020
CGAGCCTGGC TGGGAGGGTG CTCATGACAA GAGTGGGGCC ACAGGCCTCT CCTTTCATTG 1080
GACATAGTGG CCATACAAAG TGGCTGCCTT GAAATGCACC CACATACACT ATCGGTCCTC 1140
CCGGTCTAGG GAGAAAACTA GCACAGTATG TCAACAGATA 1180