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

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EnhancerAtlas ID
HS095-16917 
Organism
Homo sapiens 
Tissue/cell
HMEC 
Coordinate
chr2:121700640-121702080 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11122834chr2121701289hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MSCMA0665.1chr2:121701112-121701122AACAGCTGTT+6.02
MSCMA0665.1chr2:121701112-121701122AACAGCTGTT-6.02
MYF6MA0667.1chr2:121701112-121701122AACAGCTGTT+6.02
MYF6MA0667.1chr2:121701112-121701122AACAGCTGTT-6.02
Nr5a2MA0505.1chr2:121700773-121700788CCTGACCTTGACCTG-6.57
TCF7L2MA0523.1chr2:121700897-121700911AGACATCAAAGGGC+6.22
Enhancer Sequence
CGTATGAACA GAAACGGATA CAGGAGACAG GAGGCCTGTG AGCTCACAGC TGAGGATATC 60
TGGTCATCAG CTGAGATGGA CGTGCTCAGG TCAGAGGAAG GAGCCACCTA ACACAGAAGC 120
ACCGTAGGAG GATCCTGACC TTGACCTGGG GCTAGGGGGC ACCTTGGGTG AGAGGTCCCT 180
GAGCTGGCAC CTCTGGGAGG AGAACAGGAG TTAACTGGGG GAAGGGATGA AGAGGGGAAG 240
GGCATGACTG GAGGTGCAGA CATCAAAGGG CAAAGCTGTG AGAGGCAAGC ATGGCCAAGG 300
ACCAGAGAGT GGCATACAGG ACACAGAGGG GAGAGGCAGG CCCTGGCCAC ATGGGATTGT 360
GGCCCCTCGC CTGCTGCCAC TGAGGTCATA AGTCACCCTG AGAAGCAGGC AGGTGGTGAG 420
ATTTGTAGGC TCATATCCCC AAGTGACTGG GCCTCCTTTT CTCTTCATCA GCAACAGCTG 480
TTGGACCAGT CTGGGGGCAT CCGGGTGCCT GTGTTCCCAC CCGCTGCTGC CGCTGGCCTC 540
ACTGTGGCCA TGCCCCTGGT GCTTTGGGAC TCAGCAGTGC TGTCTGTTAA ATGGGACATG 600
AAGGAGCTGT TCCTGCCTGT GTCTGGCCCC AGCCACCAGC ACAGATCTTG GAGCAAAGCC 660
ATCTCTGGCA TGCCAAGGGT GGGCTTCTCC TCTGACTCCA ACCCCCGAGT GGGACAGCCC 720
GCCCTGATGG CTGGTGCTGA GTCTGGGTGA GTCAGCAGCC CTCAGCTCCA CATTGTTCAG 780
CTTCTCCAAG CAGGCACCGA GGCTGGGGTG TGGGGGCCCC AATCCCTGCA CTTCCTTCCC 840
TTTCTCTCAC ACCTTAAGGA ACATGCCGGT TCTTGCCCCC ACACCTTGGC TCAGGCGGTG 900
CTCAGGCCAG ATGCCCTCCT TTCTCCTCCC CAGCCCTCAA AGTCTTACTT GTTTCTCAGG 960
CAGAAGCTAC ACACCGTCCA GGTACACATC CCCCATCATT CTCACTCCCA GGGACAGCAC 1020
CCACTCCGAG GGTCTGGCAT GCTCGCTTAG GCCCAGCCAG CTGCATGCTG AGTTACACAT 1080
GGCTGTGCAG AGTGCTCATT ACCTTGACCT TTTATCTCCC ACCAAAAATC TCATGGCAGC 1140
AGATGGGGAA GGGTCCTGGG ATTTGATGCC GAAAGGTGTG GCCTGGGTCT GCTGCACTCT 1200
CTGAGCTGCT TCCATTTGCT CATCTGCTAG ATGAGCGGGG TGAGCACTAA TTGAGCACCT 1260
ACTAAGTGCC TGGTGCTACA CTGCATGCTT TCCATGCTTG GCTCATCCTA CCTCACAGCT 1320
GCCCCACCTG CAGGCAAGGG ATCCTGAGGC TCAGGGCACA TAGCACTGAG GCTGCAACAG 1380
CACCAAAGCC ATGATTCAGA CCTAGATCTG TGACTTCAGA GTCCAGATTC TGCTTATCAG 1440