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

TagContent
EnhancerAtlas ID
HS007-15148 
Organism
Homo sapiens 
Tissue/cell
BE2C 
Coordinate
chr7:2902820-2904000 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr7:2902958-2902979AGGGAAGGAGGAGGGTGAGGG+6.1
ZNF263MA0528.1chr7:2903719-2903740AGGGGAAGAGGAGGAAGAGGA+7.12
ZNF263MA0528.1chr7:2903734-2903755AGAGGAGGAGGAGGAGAAGGT+7.67
ZNF263MA0528.1chr7:2903731-2903752GGAAGAGGAGGAGGAGGAGAA+8.05
ZNF263MA0528.1chr7:2903722-2903743GGAAGAGGAGGAAGAGGAGGA+8.14
ZNF263MA0528.1chr7:2903728-2903749GGAGGAAGAGGAGGAGGAGGA+9.83
ZNF263MA0528.1chr7:2903725-2903746AGAGGAGGAAGAGGAGGAGGA+9.92
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_49131chr7:2902568-2904233Right_Atrium
SE_65520chr7:2902200-2904308Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr729032272903785
Number: 1             
IDChromosomeStartEnd
GH07I002862chr729020522905033
Enhancer Sequence
CCAGTAGCCA TGTTTCTGCC CCAACAAGTA ACCTCCTTGC CCTGTCCTGG CTCCCGGGAT 60
CCTTCCTCTG GTGGTCTGCA CGGGCCACGG CGCTCAGGGT GCCGCAGCGG CAAAGTGGGC 120
AGTGGTCGCC CGTGTTCCAG GGAAGGAGGA GGGTGAGGGC GCCTGACCTC AGAGACCCCC 180
AGAAGGTATC TGTGGGGGCA CAGATGACCA GGAGCCCTGG AGTTAGTTCC ATTTGCTGGC 240
TGTGACCTTG GAAAGCCAGC AATGATTCAG GACCGGCTGC ACAATTTGTG CAAAATGAAA 300
ATGTGGGGCC TCTTGTCCAA AAAGTATTAC GAATTTCAAA ACAGCCACAG CAGAGCACCA 360
CGCCGAGCAA GGGCCCTTCT CAGTACAGAC CCTGAGCCTC CCGAGAGTGT GAGTGCTGGG 420
GAAATCTGGG GAAAGAGGCC AAGGCTGTCC AGAGCCGAGC CCCTCCCTGG GGATTGTGTC 480
TGGGGCCCGC AAACTCCCCA GGCGGAGGGA AGAGCCAGTC CTCCGGAGAC GCTGGGCACC 540
GAGCCTCCTC CAGGCCCGGA GAACGAGCCT GTAGCCTGTC GCTGTTTGCT GAGGGCCCTG 600
ACCTCTGTGG GAACACACAG GAAGTGGTTC ATTTTCTCCC CACCAGTGAC TCACTCCCGT 660
CAGCCCTGCC CTTTCCAATC TCTGCTTCCT GTCCCTTAGC CTCAGCTTGG GTAATTCTGG 720
GCAATAGAAA GGCCAGTCTG GTTGAGTCTG AAACTGCCAT CTCACATGCA ATTTCGCACT 780
CATCTTGTCC CCCACTGAAG GGCTGGCTTA GCCTTGGCCG GAGAGCCCTG GAGAAGGAGG 840
GGAGAGGTCG GGGGGACTGG CTGCGGTCCT TCCTCTTTCT CCTGGCTTCT GGGGTTGGGA 900
GGGGAAGAGG AGGAAGAGGA GGAGGAGGAG AAGGTCTGGA GTGTCGGCAC AATAGTAATA 960
TCAATAACAA TAGCAGCTAA TATTTACTGC AAGTGGTTCT CTGGGTCTGG AGATGCTCCA 1020
AGCACTTTTC TGACCGTAAG TTATGGCATT AAGTTTTGTA ACTAGGAGGT AGGTCCTGTA 1080
ATAAGGTCCT GTTGTAATTC CCATTTTTCT CTGTTGAGGA AACAGGCTGA GACAAGGTAG 1140
GTAATGTGCC CAAGGCCACA AAATTAGGAG GTGGCAGAGT 1180