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

TagContent
EnhancerAtlas ID
HS078-04224 
Organism
Homo sapiens 
Tissue/cell
H2171 
Coordinate
chr12:52262550-52264650 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs17126180chr1252263956hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HLTFMA0109.1chr12:52264358-52264368AACCTTATAT+6.02
ZNF263MA0528.1chr12:52263112-52263133GGGGAAGAGGAGGGAGGAGGG+6.23
ZNF263MA0528.1chr12:52263114-52263135GGAAGAGGAGGGAGGAGGGAG+6.51
ZNF263MA0528.1chr12:52263111-52263132GGGGGAAGAGGAGGGAGGAGG+7.1
Number: 1             
IDChromosomeStartEnd
GH12I051868chr125226245052264384
Enhancer Sequence
GCACCCAAGA AGCAGGTACT GGGTCCCCAT TTAACAGATG AGGACACGGC TCTGAGCGCT 60
GCCCGAGGTT CCCCAGCCGA CGATAACTCC AGCCCGCCGG GCCCGAAGAG CAGAGTCCTG 120
CCTCCTCCCC ACCGGCTTCA GCCTCGGGCC TCGGCTCTGC TCCTCCCTCC TACACACACC 180
CCGGACGCGT CTGTCCAGGT CCGAAATCCA GATCCACACG TCCGTATCCC GAGGCGGGCG 240
TGAACTATCC ACCCGTGTGC ACGCCAGCCG AGCGAGTGGC CGAGGGACAC CCCCGTGCTT 300
CCCAAGGCCT GGCTCCACGA GGAGCAGAAC CCCAGCGGTG GGATTCTGTC GCGCAATGCT 360
GTGTGGCTCC GACTAGGGCC CGCCCTCCAG CAAAGAGATG CTGGTGGGTG CTCTCGGTTC 420
ACCCCCGCAC TCGCCCCAGG GGGGCTCGCG GGCCACCTGG AGCTCCCGCC CCTCGGTGGC 480
CAGGGCTGCG CGTGAAAGGG GGACGTTCGG ACGCGGGGGC GCGGAGCCAG CGCGCGAGCC 540
TCGGAGCCTC CCCCAGGCTG TGGGGGAAGA GGAGGGAGGA GGGAGCAGAT GGCAGCAATT 600
ACCGCTCGGA CCCTCCCCCG CCGTAGCCTG GGGCCGGAAG ATCGGCTCGG CAGCTCGCTC 660
CTGCGGGAGG GGCGGCGGCC TCCCCGGCCG GGAACCGGCG GGGAGGGGGT CCGGGAGGGG 720
CGGCTCTGGC CGCCGGGGCG CGGGCATCCC AGCTTCTAGG GGAGAGTGAT GTGAGGGCCC 780
GGTGGAGACA CCTCCTTCTC CCGGGACGAG GGCTGAGAGA TTCCCTTTGG AAAGGCCGAG 840
TCTCCGGCCG CCCCCACCCC CAGAGTTGTT TCAGGCCAGG GCCGGCCGCA ACCAGCTCCG 900
GGCCTTTAGG TCCTCAAAGT TCCGAAGATT TTCAGGTCGA GCCAGTGGCC CAGGCTAGGG 960
AGAGGGGAGC TGTACGGTTG TGCAGGTTGT GACCTATACA AGGTGGGAGG CGTGGTTGTG 1020
GGTGAGTGGG ATTCCAAGCT CGGCCTTGGC AGGTGCTGAC TCGTTCTGAA GGAGGGCAGG 1080
GGGCACCGTT TCTCACAAAG GTCTCGGATG AGCCAGCCTG GCCTGCCCTT GATTTAGGGC 1140
TGCTGAGGGT AGACACAGTG GGAGAGCAAA TGGCTAGGGT TGGCCCCTGT GGGTCAGGGC 1200
CAGGGCTAAA GAGGACAGGG GGACTCTCCT GGCCCAGAGT AGAAACAACT GGATCATCTG 1260
GGCTCCCTGG GCCTTTCTTT CTTCTTGAAT TCCTCTCCCA CCCTCACCCT GAATCTTGTT 1320
CCTCTGTCTC TAACATAGTT CCTAAAACAG CCCCTGCCCC TGCCCCCACT CAACTGCCCA 1380
AGCTCCTGTT ACTTCCCTGC ACAATCGAAA AGACTCCTGT CCGCTCTCCC AGGGTCCCCA 1440
ACAATCAGTT CACACTGCAG GCAAAGAGAC CTTTAAAAAT ACAAATCAGG AAAACACCAG 1500
GGCATGTGAT TCCTCGCTTA ACAGCCACCC ACAGCTTCCC TGCAAAGGAA GCCCAAACCT 1560
TTTCCCCCAG CCCCTACCTA CACAGACAGA CCTCTCTTCC TATCCTTCTC CCCACTGCCC 1620
AGACACTGCT TACACTGGCT GCCTTTCTGT TCATTGAACT TGATAAGCTT TCCCCCACCT 1680
CTGGCCTTGG CTTTGCTGGT GCTTTTCCTG GATCGCTCTG CCCAGATCCT TCCCAGGAAC 1740
GTCACCTTCC CATCATCCCT GACCACAATA ATAAAGCAGC CCCATCTGCC TGATCCAGTC 1800
TGTCACTTAA CCTTATATAT TTCTTCCACT GAACTCACCA CATTCTGTAA TTATCTTTCT 1860
TATTCACTTG GTTTGTGGTC TGTTTCACTT ACCAGAATGT CAGCTTCATG AACGCGGGGA 1920
CCTTGTCTTT CTTGTTCTCT AGCACAATGC CTGGTGCAAA CCAAGAAGCA CTCAGTACAT 1980
GCTCCATACA TTCCAGGAAA GGAGTCCCTG GGACCAAACT GGATGCTAGT TCATCTGGTC 2040
ACCTCCGAGA GGGCTTCTCT CTGGGTGGGG CCAGCTACAA ACACCTGTAC TCACCTGGTA 2100