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

TagContent
EnhancerAtlas ID
HS108-21337 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr2:3634140-3635570 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs4850047chr23634753hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
JUN(var.2)MA0489.1chr2:3635275-3635289CTGAGTCATCTTCT-6.53
ZfxMA0146.2chr2:3634388-3634402GAGGCCGAGGCGGG-6.01
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr236350053635346
Number: 2             
IDChromosomeStartEnd
GH02I003583chr236314373634339
GH02I003587chr236346433636301
Enhancer Sequence
GTCCTCCACG GGCAGAGGGG ATGGCTGCCC AAAGGACATG ATGTGATGGG CCTGGCCTGG 60
GCACACTGTG CTCCACACCC CACTTCAGAC AATAGAGGCA GATTCACCAT GAGGCCAATA 120
AAGATCCGGC TGGAGAGGCC TTAGCATTGA GTTCTGTGGT CATATATTTG TATAAAATTA 180
GCACAAATAA AATATTAAGC ACAATGGGCC GGGTGCGGTG GCTCACGCCT GTAATCCCAG 240
CACTTTGGGA GGCCGAGGCG GGCGGATCAC GAGGTCAGGA GATCGAGACC ATCCTGGCTA 300
ACACGGTGAA ACCCCGTCTC TACTAAAAAT ACAAAAAATT AGCTGGGCGT GGTGGCGGGC 360
GCCTGTAGTC CCAGCTGCTT GGGAGGCTGA GGCAGGAGAA TGACGTGAAC CCAGGAGGTG 420
GAGCTTGCAG TGAGCCGAGA TCGCGCCACT GCACTCCAGC CTGGGCGACA GAGCCAGACT 480
CTGTCTCAAA AAAAAAAAAA AAAAAAGCAC AATGAGTGAA GACCGCTGTC TGGTTCCTCT 540
GTCACAGCCT CCTGCTGAGT GGTGCCGATG CGGCCCAGGC ATCTTTGCAT CCTGCTGAGG 600
GTTTCCCCAC CTTGGCACTG TTAGCTTTTA GGGCTGGAGA GCTCTGTGCT GTGGGGCCAT 660
CCCATGCATT GTAGAATGTT TAGCAGCCTC CCTGTCCTCT CCCACTAGAA GCCAGTACCA 720
TGTCCCCAGT TGTGACAACT AAAAATGTCT CCTGCACATT GTCAAATGTC CCTGAGCCCG 780
AGGGGTGGGG AGAACAAACT GACGTTGAGT TGGGGTTATA TTATTTTGGA TTTCAGCTGG 840
ATATGCTGGG TGGTTCATGG TGCAGGAGGA GGTCATGAGC TACAAATTGG TCAGTGGTGT 900
GGTCATTTCA AAGACTAGGA TTACTCTGAA CAAAACAAAC CAAAACCCAA TCGTTGAGAT 960
GCCTGAAATC AAACACCTAG TATATGAAAG AAAACTGATA GAGGTTTCCC CAGACTTGAC 1020
AGCTATCCAA AAACTGTTCA TGGCGTCACT GATAAAGGCT TGTGGAGCTG AAGTAAACTG 1080
TTTTGAAGCT ACCAATAAGA AGATATTTAA ATAACCATGC AAGAAAGAGC AAATACTGAG 1140
TCATCTTCTG TTCTCTTTGT AGAAATTTGT GTTCACGGGA GCAGGCAATG AAAGAATATA 1200
CAGCCAAATA ATATAAAAAC GTAAGGGCTG GGCTGGGTGC GATGGTTCAC ATCTGTACTC 1260
CCAGCACTTT GGGAGGCCGA GGTGGGTGGA TCATGAAGTC AGAAGAGCGA GACCATCCTG 1320
GCTAACACGG TGAAACCCCG TCTCTACTAA AATACATAAA ATTAGCCGGG TGTGGTGGCG 1380
GGCGCCTGTA GTCCCAGCTA CTCAGGAGGC TGAGGCAGAA GAATCGCTTG 1430