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

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EnhancerAtlas ID
HS073-00343 
Organism
Homo sapiens 
Tissue/cell
GM19238 
Coordinate
chr1:31241550-31242740 
Target genes
Number: 3             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs74340846chr131241886hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
STAT3MA0144.2chr1:31242676-31242687CTTCCCAGAAG-6.14
Number of super-enhancer constituents: 8             
IDCoordinateTissue/cell
SE_12625chr1:31241550-31241729CD34_adult
SE_12625chr1:31242092-31242244CD34_adult
SE_13496chr1:31240733-31243188CD34_Primary_RO01536
SE_20783chr1:31239849-31243479CD8_Memory_7pool
SE_39886chr1:31240810-31243613K562
SE_53612chr1:31241288-31242640Spleen
SE_61144chr1:31205054-31253025HBL1
SE_62248chr1:31201545-31253778Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr13124179531242280
Number: 1             
IDChromosomeStartEnd
GH01I030768chr13124082531243157
Enhancer Sequence
CTGAGACCTG AGTTTCTGAT CCAGTCTGGG AGCCAAAGCT GTGAGGAGGA ATGTGTGTTG 60
AGCAGCAGCT CTGGACCTCA CTCTCTTACC TTACCTGGTT CAATCCTCAC AACAACACAA 120
CCCAGTGATC CAGCATGGCC AGATGACCTT CCGTTTTAGA GATGAGAAAA CCAAGGCTCT 180
GAGACGTTGA GCCATTTGCC CAAGATCCTA GAGCCCAGAT CCTAAGTGGC AAACTGGAAC 240
TCAAATGCTG GCCTGGGATG AGCAGAAGCA GGTTCTCAGC TTCTTCAAGG GTTGGAGGGG 300
GCTGGGGAGG TTGTGTCAGG GTGTGGGCAG CAGTTGGTGG TCAGTGACTT TCCCTTGTGG 360
CAGGAAGGAG AGGTAGGGGA AGCAGCTGGA GTTGGGAGAT AGGAGGCTGA GGCAGCAGGA 420
CCCACAGATA AGGCAGGAGG TGAGCAGGGG CGGGTGTGCA CATCCCGGCA GCTGGAGTGT 480
AGATGAAATC TCAGAGAGCC CGGCAGAAGG GCTGGACCAG GGACCACGTC ACTCCCAGGC 540
CTGACCACTC CCTGCTTCTC CAGGCCACGT CTCACCCCTG AGCCTCGCAG CAGCCGTCAC 600
GGTACTTTCC TGGGCCTGGA AACGGCAGCC CCAGCCAGGC CTCCCTCTTC TCCAGGGTCA 660
GATACAGGGG GCAGTGTGAC ATGATGCGAG AGCCGGGGCT CTGTCCTTCT GCTCTGCCTC 720
AGGCCTGCTA CACCTGAAAG CAGTCAGCCA GGCCTGCAGA CACTCGGGGC TTCCCAGGAC 780
CAACACGGTC CCACCATCTT GTTGTTTCAC TTCGAATGTC TTCATGACAG GCACACACTT 840
TCCAGCTCTC CACCGTCCCC GCCTCTCCCT ATTGTCCCAC AACTTGTCAC ACCCCACATT 900
TACCTTCTCT ACCTGGCCCC TAAAGAATTT CGATTTTGAG GACCTGAATT AGTTGAGCGG 960
ATGCACTGAA GGTCAAAGTT TGTAATTTTC AGGGAGAAGG AACCTTTGAG ATATAAGGGC 1020
CCAGAATGAA GCAGTAACAT CCCCAGAGTC CCACTGCAGA GCGAGACAGA AATGGGACTA 1080
GAACTCCTGA CTCTCAGTCC AGTGCTTGCT GACCTGACTT CTGCTGCTTC CCAGAAGCCT 1140
CAGGGAGGAA AACAGAAACA ACTGAAGGAA AAGAATGGAG AATTCACAGT 1190