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

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EnhancerAtlas ID
HS048-03240 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr1:207413980-207415340 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSMA0476.1chr1:207414272-207414283TGTGACTCATT+6.62
PBX1MA0070.1chr1:207415240-207415252ACATCAATCAAT+6.44
TBXTMA0009.2chr1:207414261-207414277TGGCACCAAAGTGTGA+6.04
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1207414055207415220
Number: 1             
IDChromosomeStartEnd
GH01I207239chr1207413145207418270
Enhancer Sequence
TCTTGTAGTA AAAATCAGCA TATTTATTAT TATTATATTA TTATTCAAGT ATTATTTCCC 60
ATGAATTATA ATTATGTACA TAAACAGCTT ATCTTTTACT GCCTTTTTTC AGAGACATAA 120
CACCAGGCTG AGTGTGGCTT TTGGCTGATT GAAAACCATG CAAGCATTCT TCAGGTCTGA 180
TGGAATCTTG CTGTCTGTGT ATGTTCCCAC TTGCAGCCAC ATGCTCCTGC ATGCTTTTCA 240
GTGCTTCAGG CACCACATTT CCCTCTTTTA ACAGACCAGA ATGGCACCAA AGTGTGACTC 300
ATTAGGTGAC TTAGGTAAAT CAGGAAAAAC AAAAAGGAAT GTCCCACTCA AATATTGTCT 360
GAGTAATTTT GTCAGGCCTG TCTGTATTCT TGAGGTTTTT TTTTTTTTTT TTCCGTATTT 420
CTCTTTCCCC CTCAGGCTTT AGAACTTTTG GAAGGAAATG TAACTTTCCT CATCAATTTT 480
GTTTTGTTTG TTTTTTAATT TCATCCTTCT GTTGGCAGTC CAAATTCATA ACTGAAGCCA 540
CACCTTGTCC TAAGTAGGCA GTGCTGCTCA GGATGGCTTT CTCTCACGCT GTGATTTCCT 600
GACTCGAGTG GATCTCACAC TCAGACTTAT CACACTCAAG GTTTGCTTTA AGGGTGACTG 660
AGCCTGCCCA CTCTGAACCA AAGTCCTTTT TTTCCATCCC TTATTTGTTT TTTCACTCAA 720
AAATGAATTA CTTACATTCC TAGATAACAA TCTCTTTTAA GTACAGCTCC TATCCTGTAA 780
GGAAAAGATT AGGGTTCTAT TGCTAAATGG CTTCAGAGTT CCACAAGGTT ACTTACTCCT 840
TGCATCAGAG CCCCTGATGC TAAAATTGAA GTTTTGAGTG TCCTTTGACT CAGTTGATTC 900
TAGGAACCCT GATTCCACCC TCTTGCCCTG AGCTCTTCCT TAATGCAGAG CTTGGTCTTG 960
ACCTGACTTT GCCCCAGGGT GTAGCTGCTA CTGGCTATTG GACAGCTGAC CTCCAGTTTG 1020
GCAGAGGCTG CTGCTAGTTC TCTCTCTTTC CTTTAGTTGT TTCTAGGTGG AATCTGTGAC 1080
CTTCGGGCTT CTGTCAGTGC AGGTCAACAT GTACCATGAG GCCTGCGTCA GGGAGCAAAC 1140
CACCCTCCCA TCCCTGTATC TCATGCCTAT CCAGCCTACA CCGTGAGCCA GGCATTCCTA 1200
GTGCACAGGG CCCCAGGAAA GCCTGGGTAA AGTGCACAAT CAATGAAAGG AAGGTAGTTT 1260
ACATCAATCA ATTGCAAAGA TATTTATTCC ATGTTAGGAA TTTTATAAGT ATGGTCAAAT 1320
TGTAGTAATT TACACCAATT TGTGGGAGGC ATAATAAATT 1360