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

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EnhancerAtlas ID
HS044-08753 
Organism
Homo sapiens 
Tissue/cell
Fetal_kidney 
Coordinate
chr3:15334280-15335210 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr3:15334898-15334916GGGAAGAAGGAAGGCATG+6.33
INSM1MA0155.1chr3:15334856-15334868TGCCCCCAGGCA-6.04
Stat6MA0520.1chr3:15334750-15334765AGTTCCCAGGAACTG-6.24
Number of super-enhancer constituents: 11             
IDCoordinateTissue/cell
SE_00079chr3:15331987-15343946Adipose_Nuclei
SE_00929chr3:15334247-15335409Adrenal_Gland
SE_09444chr3:15331982-15339136CD14
SE_11008chr3:15324524-15353343CD20
SE_15021chr3:15331985-15335299CD4_Memory_Primary_7pool
SE_18453chr3:15331979-15335447CD4p_CD25-_Il17-_PMAstim_Th
SE_19507chr3:15332067-15335156CD4p_CD25-_Il17p_PMAstim_Th17
SE_38835chr3:15332090-15338571HUVEC
SE_45914chr3:15334319-15335387Osteoblasts
SE_47061chr3:15334373-15335080Ovary
SE_62482chr3:15309098-15428510Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr31533461515334919
Number: 1             
IDChromosomeStartEnd
GH03I015287chr31532850915339408
Enhancer Sequence
GGAGGCGGAG GTTGTGGTGA GCCGAGATCA CACCATTGCA CCCCAGCCTG GGCAACAAAA 60
GCGAAATTCC ATCTAAAAAG AAAAAAGAAA AGAAAACCTC AAGATCAGCA ACACTCTCCC 120
TGCTCCAGCC CCAGACGCCC GAGGCAGAGC CAGCCAAGCA GGAGGTGCAA CCCTTCTGGC 180
AGAAGCCCAA AAATCTACTT GTGTGTGTCA GGAGCCTTTG ACCTGGGTCA AAAGCTGCAA 240
CACATCTCCT TCCTGACCCC ATCCTAATTC AAGATTCCAA GTTTCCAAAG TGCAGCTGCT 300
TCTTTCCCAG AATCTTCAGC CAAGACTGTC AGGCAGGATG TGATCTTTCA GGCGAAGGAG 360
AGTTAAGAGT CCATGCTCAG TTCTTGCCAT AAATCTCCAG GAACTCTGCT TTGAGACAGA 420
TGCCCTGTCA TTCCACTACG TGCCCTTACT TTGGGCAGCA GGAATGACGC AGTTCCCAGG 480
AACTGGCCTG TGGCCACCCA GGGGGAATGT GACCAGGGCC ACAGGGAAGA ACGTCACTGA 540
GCCAGACCTC CTCACCCAAA GTCCCGTGGC AAGAACTGCC CCCAGGCAGG CAAGTGGCTC 600
TGCAGAGATA AAGTGACGGG GAAGAAGGAA GGCATGACAA AGCCACACTG AAGTCCTAGC 660
AGGAACAGGG CACCATGAGG GGAAAGTTCC CAAGGACTCC AGATTCTTGG AACAAGAGCT 720
TCTCGGAACA AGAGCTTCTC AGTTACCCTA GCCAAGAAGA GGCAGGGGTG TGCAGGGAAA 780
TAACTGCACC AATGAGCTCA AAAACTGCCT TTAGTCCTAA AAGCCCATTC TCCTCAGATG 840
TGCCAGAGTG TCTTTCAGAT TTGCAAATAG TCATAAATGC CTCCTATGTG CCAGGCACCA 900
GCCAGAACCA GGTAGACTTG GTTTAAACCT 930