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

TagContent
EnhancerAtlas ID
HS048-01280 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr1:48340870-48342630 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs10493130chr148341005hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MAFGMA0659.1chr1:48341613-48341634TTTGTGCTGCATCAGCACATG-6.08
NR2F1MA0017.2chr1:48342143-48342156AAAAGGTCAAGAG+6.25
Nr2f6(var.2)MA0728.1chr1:48342137-48342152TAAGTCAAAAGGTCA+6.04
RELMA0101.1chr1:48342223-48342233GGAAATCCCC-6.02
ZNF263MA0528.1chr1:48341372-48341393GAAGAAGGAAAGGAAGAAAGA+6.29
Number: 1             
IDChromosomeStartEnd
GH01I047875chr14834144748342330
Enhancer Sequence
GTTCCAAGTT GTTAAAAGCA TGTTAGCACT CCATGGAGAC TTCTTCCTGA GTACAGTGGA 60
AGACTGAAAA TTTCCTACCA CAATAGGAGC TGAGAGTGTT CTTTAGTATT CACGCACAGC 120
ACGCGGCAAC ACTAGATATG CTGCCCTTAA AGCTAAAAAG TCCTAGATTT CAATAAGCTT 180
TCTCTTAAGC TAAGAAGGAC AAAGTGGGCT GGGCGTGGTG GCTCATGCCT GTAATTCCAA 240
CACTTTGGGA GGCAGAGGCA GGAGCACCGC TTTACCCCAG GAGTTCAAGA CCAGCCTGGG 300
CAATATGGCA AAACCCTGTC TCTACAAAAC ATATAAAAAT CAGCTGGGTG TGGTGGTGCA 360
TGTCTGTGGT CCCAGCTACT CAGAAGGCTG AGGTGGGGGC ATCACTTAAG CCCAGGAGAT 420
GGAGGTTGCA GTGAACCATG ATCGTGCTAC TGCACAACAG AGTGAAACCC TGTCTCAAAA 480
AAAAAAAAAA AAAAAAAAAA AAGAAGAAGG AAAGGAAGAA AGAAAGAAAG AGCAGAAAAG 540
AAAAGGACAA AGTGACTTCT TCTACCTGCA GGGAGGTCAT TATACTTCCT CAATATCCCA 600
AGTCCCCTGA GAGTTCTGAT CCTGGCCCCC AGGTGAGTTC TCAACCCAGC CACAGATCAG 660
TGCTGGCTGT GGCCACAGCC CTGGCCTCTC TGCACACTCA CATCTATTTA TATTTGTGTT 720
TCCCACTGAA CCTTCCACAG TGCTTTGTGC TGCATCAGCA CATGATGTAT ATTTACAAAA 780
TGAACATGTG AAAGAACAGT GTCACAAACA AAGCCAAGAC AGACAGATAT ATTTTCCACA 840
ACCAAAGGAA ATGGTGCTCC CTCCAGCCCA CTGGAGGTCC CAGCCTCCCA GAAGGTCCAC 900
TCCACTACTC TACAGTAACA GGAATGAAAA GAAGTGTCTG GAGTCACACA AGCCTGACTT 960
GTCACTGAGC TTGAACAAGC GCGTCACCCT CTCTAAGCCT CAGTTCAGTC AACTCAAGTG 1020
GGGAGCATAA CCCTGAGATC ACAGGGCTGC TGAGAAAAAT CAAATCAAAT AACTCATGGG 1080
AAAAAGCCAC ATAAACCCGA ACATAGAACA GTGTGATGTC GTCATTGCCC TGACTTGAGA 1140
GAACAAAGCA CAGATCCAGT GAAGGGACTT CCCATGGCAA CCTGGGAACC ATAACTGTCT 1200
CTGACTCCTG GCCCAGAGCA CAGACTCTAG GTTAGCCAGC CAACCCCATC TCTGCAGCAT 1260
TAATCATTAA GTCAAAAGGT CAAGAGGCCT CTAGCTGGGA GACAGACTAA GTACCTACAA 1320
GTGGGGCTTG TGTATGGTGG TGGGGAGGGG CTAGGAAATC CCCGCAACTT CAGGATTCAG 1380
AGCTCTCTGG AGAAGTACAG GTTCATGGAG AAGGAAGCCA TAGCCCTGTT CCTCAGAAGC 1440
CTACCTGCAA CATGCCAGAA ACTTCCCCTG GCCCAGCCGG GGGGCCCACA GCCTCCAGCA 1500
GTGCTGGGAG GGGTTCCGGG AGGGAGTGAG TGCTGCCCCA CTCAGAGAGC ACTGACAGCA 1560
GCAGGCAGCA CTCCTTCATG TCTCTGTTTA CTCTTTATAT ACGCACATAC TAAGCACCAA 1620
CTGTTTGCCA GGCACTGGGC TACATGCTAG GTCATTCATG CATTCGTTCA TCCACTCATC 1680
ATTCCTTCAA TAACAACTGT CTGTCAAGCT CTTCCTGTGT GCCAGGCACT GTGCTAGGCA 1740
CTGCAGATCT ATAATAGTAG 1760