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

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EnhancerAtlas ID
HS051-12756 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr17:81029120-81030400 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ESR2MA0258.2chr17:81030106-81030121GGGTCAGGCTGCCCC+6.08
EWSR1-FLI1MA0149.1chr17:81029816-81029834CTTTCCTCCCTCCCTTCC-7.64
ZNF263MA0528.1chr17:81029796-81029817CCCTCTCTTCTTCCCTCCATC-6.02
ZNF263MA0528.1chr17:81029823-81029844CCCTCCCTTCCTCCTTCCTTT-6.34
ZNF263MA0528.1chr17:81029792-81029813CCTTCCCTCTCTTCTTCCCTC-6.73
ZNF263MA0528.1chr17:81029816-81029837CTTTCCTCCCTCCCTTCCTCC-7.56
ZNF263MA0528.1chr17:81029819-81029840TCCTCCCTCCCTTCCTCCTTC-9.39
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr178102942581029675
Number: 1             
IDChromosomeStartEnd
GH17I083072chr178102994181030090
Enhancer Sequence
TGTACTTAAA AAGTATGTTT TTAAACATTT TAATTAGCTC TCTAGACTCA AATAATCATC 60
TTCTTCACCT TGTTTTCTCT GTGACACGCA AAAGGCTGGC AGGCAGGAGG CTTCTCAGAG 120
TCAGGAGGGC TGGGGGGGAA GGTGCTGTCC ACCAACATGT TCTGGACAGG ACGCAGACAC 180
CAGGCGCCCC ACGGCCCTTC ATGCTCCGGA GGGTAGAACA GAGCCAGAGG GTGGTGAGGA 240
AGGGGCAGAT CCTGGTGGCT GCAGCCACTG CTGTGAGGGG ACGGGGACAG GGCTGCTGAG 300
GTCGAGGCAG GGAGTGGGGA GGCCGGAATG GGAGGCCCAT GCTCCAAAGT ACATAGGAAG 360
CTGGAGCTTC CCTCCCACTG AGCTGGGCCA TGAACCTGCC CACGACTCTG TGGGGTTGGC 420
ACCATGAAGT CGCTCTCAGA TGGGGAGCTG GAGGGTTGAT CGCCACCAAG TCACGCAGTT 480
TAGCAGTGGG CACTCCTCGA GCCAACCTGC ACCACCTCAC TAAGCCCAGC ATGGGCTCCC 540
AGTGCCCCTC GGCCCACCTC CCTATCAGCC ACGCCCTGGG CCTGGCCCCC TGAGAGGCCC 600
CATGAGGCTG CAGTTGTTTT CTGGGTAAAC TGTGTCCCCC CCCATCATTC ATAACAATCT 660
CTCTCTCTGT CTCCTTCCCT CTCTTCTTCC CTCCATCTTT CCTCCCTCCC TTCCTCCTTC 720
CTTTTTTCTT TTTTTTCCTT TTTAAATAAT TTGTTTTCTC ATCATAATAG CAATACCTAG 780
TCATTGTAGA AAAATTGGGG ACGATTAAAA TTCCACCGTG GAGTCGAGGG GAGACTTCCC 840
CTGGCTCCTG TCACTGTTGC CACACTGCAT ATAAAGATCT GTGGTTTTGT TTCTTCAGTT 900
CACGTGACCT CATCGCTTTA CTCTCTCACT GGAGTCCCTT GTGAGCCTGG TGACAGCAGC 960
CTCATGACCC CAAGCTCTTC CACGTGGGGT CAGGCTGCCC CCAGCCTCCT GCCCTGACTC 1020
CTGCTGGGTT GGGTCTCCTT GCACCCCCAC ACAGTGCACA GTGCCAGCTG CTCCTTTTCC 1080
TCACCCTTGC TTGAACAGTT GTGCACGCAT GTAGGTCACC TCTTCCAGGC AGCCCTACAG 1140
GAGTGCACCC CACCAACACT GACAACCCCC CAGACAGTGC TTAAAGACTG AAACTGCCAG 1200
CTAGGATTTG GGGAGGGGTC CCTGCCTCTG TGGGTCCTGT CTGGCTCTGG CCCAGGCTGA 1260
CAAGGAGGAG CATCTATGCG 1280