EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS050-01217 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr1:25056500-25057960 
TF binding sites/motifs
Number: 18             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NR2C2MA0504.1chr1:25057716-25057731TGAGGTCAAAGGGCA+6.86
Nr2f6MA0677.1chr1:25057717-25057731GAGGTCAAAGGGCA+6.65
RxraMA0512.2chr1:25057717-25057731GAGGTCAAAGGGCA+6.62
ZNF263MA0528.1chr1:25056836-25056857GGAGGGGGAGGGGAGGGGGAG+6.01
ZNF263MA0528.1chr1:25056847-25056868GGAGGGGGAGGGGAGGGGGAG+6.01
ZNF263MA0528.1chr1:25056823-25056844GGAGGGGGGAGGGGGAGGGGG+6.03
ZNF263MA0528.1chr1:25056824-25056845GAGGGGGGAGGGGGAGGGGGA+6.08
ZNF263MA0528.1chr1:25056810-25056831GGAGGGGGAGGGGGGAGGGGG+6.37
ZNF263MA0528.1chr1:25056830-25056851GGAGGGGGAGGGGGAGGGGAG+6.65
ZNF263MA0528.1chr1:25056844-25056865AGGGGAGGGGGAGGGGAGGGG+7.23
ZNF263MA0528.1chr1:25056839-25056860GGGGGAGGGGAGGGGGAGGGG+7.49
ZNF263MA0528.1chr1:25056850-25056871GGGGGAGGGGAGGGGGAGGGG+7.49
ZNF263MA0528.1chr1:25056807-25056828AGGGGAGGGGGAGGGGGGAGG+7.67
ZNF263MA0528.1chr1:25056813-25056834GGGGGAGGGGGGAGGGGGGAG+7.97
ZNF263MA0528.1chr1:25056833-25056854GGGGGAGGGGGAGGGGAGGGG+8.18
ZNF263MA0528.1chr1:25056820-25056841GGGGGAGGGGGGAGGGGGAGG+8.19
ZNF263MA0528.1chr1:25056802-25056823GGAGGAGGGGAGGGGGAGGGG+8.37
ZNF263MA0528.1chr1:25056827-25056848GGGGGAGGGGGAGGGGGAGGG+9.41
Number of super-enhancer constituents: 7             
IDCoordinateTissue/cell
SE_03668chr1:25056864-25057733Brain_Angular_Gyrus
SE_04517chr1:25056867-25058172Brain_Anterior_Caudate
SE_05379chr1:25056417-25058249Brain_Cingulate_Gyrus
SE_06312chr1:25055251-25058327Brain_Hippocampus_Middle
SE_07165chr1:25055397-25058025Brain_Hippocampus_Middle_150
SE_08484chr1:25056421-25058225Brain_Inferior_Temporal_Lobe
SE_41323chr1:25056830-25057633Left_Ventricle
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr12505688025057476
chr12505661725056885
Number: 1             
IDChromosomeStartEnd
GH01I024730chr12505687925057792
Enhancer Sequence
CTGGGAGACC AAAGTGGGCG GATCACCTGA GGTCAGGAGT TTGAGGCCAG CCTGGCCAAC 60
ACAGTGAAAC CCTGTCTCTA CTAAAAATAC AAAAATTAGC AGGGCATGGT GGCGGGTGCC 120
TGTAATCCCA GTTACTTGGG AGGCTGAGGC AGGAGAATCA CTTGAACTGA GGAGGCTGAA 180
GCAGGAGATT GGCTTGAACC TGGTGGCAGG GGGGTGGACG TTGCAGTGAG CTGAGATAGC 240
GCCATTGCAC TCCAGCCTGG GCGACAAGAG CCAAACTCCA TGGTGGGGGG AGGTGGGGAA 300
GCGGAGGAGG GGAGGGGGAG GGGGGAGGGG GGAGGGGGAG GGGGAGGGGA GGGGGAGGGG 360
AGGGGGAGGG GACTCCTTCT CAAGCCTCAC CTAAAAATGA AGAGGCAAAC AAGGTGGGAA 420
AAAAATAAGT GTCGAGCTCA ACCCTTAGGA CCCTGGCCAT GTCTGCAGTC AGCTCAGGCA 480
AGGCTGTTGT CCTTCTGTAA TGGACTGTCC CTGGTGCGCT CTCAGACGCA GCAGGACACG 540
ATGCGGCAGG ACCCAGTGTT CCACGCAAGG ACCTGCAGTC CTGGTTCAAA TCCAGACACT 600
GCCATAGGAA GCTTAGCTCT ACGTGAGGAG ATTAGCGACT GTTCCATGCG GGAAACAAAC 660
CAACCAAGCC AAAGCCTGCA AGTCTCTCCC AAGCTGCCAG CAAGTGAGCC AGGTGGACCT 720
CCAGGGCGTA GGATGCAGCT GGGAAAACAA CCGACCCGCT GCTTTTCCGG GTCCCTGCGC 780
TTGCTGCGTC TCCTCTGGCT GCAGAGACTC AGCCCGGCTC AGAGCTGGGG AACTCGGTTA 840
TTCTTTTGAA GCGTCAAGGG CACTTGTCAG CTTTGAAATA ATACATTTGC TGGCTTGAAT 900
TTCAAATAGC TTAACGCCCC CTGTGCTACC TAGCTGTGAT CTGAAGGACT GACTGTTCAG 960
GCCTTCAAGT ACCAAATAAA TGAACCATGA GACTCCAGCA ATGGAGAAGA AATGTCCTTA 1020
TTCAAACCAA ACTTTGCAAA TGGAAAGAAT TGTTAAGTTT TGCTCTGTTG TGGCAGGGAA 1080
GCAGCTGGGA AGTAGACCAC CCCTTGCATG CTCTGGGGGC CAGAGCTGGC TGTACTTGCA 1140
CCTTTAGGCA GTAGGAAATG CACCCCAGCT CTGTGGTGTG AGCCACTTCT CCGTGATGAA 1200
GGTCATCTTC ATATTCTGAG GTCAAAGGGC AAATGGCAGA GTGGGCATCC GTGGGGAGAC 1260
TGCTGGACAC AGGGCACTGC CCACAGAGAG GTGATGGGTG ATAGGAGTGG GGCAGGACAG 1320
CATAGCAAGG TGCAGCATCT GGAGTCAGAA CAGACAGGTT CAAATCCCAG CTCTGCTGCT 1380
TACCTACTAA GCTGTTTGAT TTGGGCAAGT GATTTAATCC TGCTAAGCCT CAATTTTCTT 1440
CTCTGCAAAA TGGGAGTAAT 1460