EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-53708 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr22:43548230-43549380 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs138177673chr2243549116hg19
TF binding sites/motifs
Number: 29             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr22:43548994-43549012GCTTGCTTTCTTCCTTTC-6.21
EWSR1-FLI1MA0149.1chr22:43549135-43549153TTCCCCTTCCTTCCTTCC-6.42
EWSR1-FLI1MA0149.1chr22:43549143-43549161CCTTCCTTCCTTTCTTGT-6.64
EWSR1-FLI1MA0149.1chr22:43549002-43549020TCTTCCTTTCTTCCGTCC-6.8
EWSR1-FLI1MA0149.1chr22:43549081-43549099CTTTCTTTCTTTCCTTCC-6.95
EWSR1-FLI1MA0149.1chr22:43549022-43549040CCTTCCTCCCTCCCTCCC-7.28
EWSR1-FLI1MA0149.1chr22:43548998-43549016GCTTTCTTCCTTTCTTCC-7.2
EWSR1-FLI1MA0149.1chr22:43549006-43549024CCTTTCTTCCGTCCTTCC-7.8
EWSR1-FLI1MA0149.1chr22:43549014-43549032CCGTCCTTCCTTCCTCCC-7.91
EWSR1-FLI1MA0149.1chr22:43549097-43549115CCTTCCTTCTTTCCTTTC-7.97
EWSR1-FLI1MA0149.1chr22:43549010-43549028TCTTCCGTCCTTCCTTCC-8.2
EWSR1-FLI1MA0149.1chr22:43549018-43549036CCTTCCTTCCTCCCTCCC-8.32
EWSR1-FLI1MA0149.1chr22:43549085-43549103CTTTCTTTCCTTCCTTCC-8.46
EWSR1-FLI1MA0149.1chr22:43549089-43549107CTTTCCTTCCTTCCTTCT-8.46
EWSR1-FLI1MA0149.1chr22:43549093-43549111CCTTCCTTCCTTCTTTCC-9.47
EWSR1-FLI1MA0149.1chr22:43549139-43549157CCTTCCTTCCTTCCTTTC-9.6
Foxd3MA0041.1chr22:43549165-43549177GTTTGTTTGTTT+6.32
IRF1MA0050.2chr22:43549053-43549074CCCTTCTTTCTCTTTCTTCTT+6.22
IRF1MA0050.2chr22:43549111-43549132TTTCTCTTTCTCTTTTTTTCT+6.3
IRF1MA0050.2chr22:43549066-43549087TTCTTCTTTCTCTTTCTTTCT+6.77
IRF1MA0050.2chr22:43549105-43549126CTTTCCTTTCTCTTTCTCTTT+7.67
ZNF263MA0528.1chr22:43549081-43549102CTTTCTTTCTTTCCTTCCTTC-6.02
ZNF263MA0528.1chr22:43549127-43549148TTTCTTTCTTCCCCTTCCTTC-6.02
ZNF263MA0528.1chr22:43549085-43549106CTTTCTTTCCTTCCTTCCTTC-6.03
ZNF263MA0528.1chr22:43549002-43549023TCTTCCTTTCTTCCGTCCTTC-6.32
ZNF263MA0528.1chr22:43549010-43549031TCTTCCGTCCTTCCTTCCTCC-6.37
ZNF263MA0528.1chr22:43549017-43549038TCCTTCCTTCCTCCCTCCCTC-6.86
ZNF263MA0528.1chr22:43549021-43549042TCCTTCCTCCCTCCCTCCCCT-6.9
ZNF263MA0528.1chr22:43549026-43549047CCTCCCTCCCTCCCCTCCCCT-7.32
Number of super-enhancer constituents: 4             
IDCoordinateTissue/cell
SE_23668chr22:43546568-43549082Colon_Crypt_1
SE_24969chr22:43546648-43549190Colon_Crypt_3
SE_26727chr22:43546429-43549260Esophagus
SE_54378chr22:43546505-43549380Spleen
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr224354917943549267
Enhancer Sequence
GAGAAGCGGG GGCTTCCTGC TGTGAACGCG CTGCTGGCCA GGGCAGCTGC CAGAGGCCAT 60
GGCCTGGCGT GGGCCTGGAG CCCCTCTGGC CAGCCTGCCA GGGGCCAGGG CTACGGGATA 120
CCAGCAGCGT GCCCTGGGCT GGATGGCAGG AGAGACAGGA CTTGAGGCTG TCCCAGAATG 180
GGCTCAGGCA GGGCGAGGAT ATCAGGGGAG GTGGTGTACA GGAAGCAGCC GCCCAGCTTG 240
CCTGGCACAC AGCAAGCCCT GCCCATGAAG GCCTACTGCC AGAACAGTGG GCGAGGCCCG 300
GCGTCTCTGT GGAGTCGGTG GGGCCCGGGA CAGGGCAGCC TGAGGCAGGT TTCCACTGGC 360
GGTGAAAGGG GCCGTGTGGC AAGGACAGGA GAGCCAGCCT CAGCCCAGCA GGGGAAGGCG 420
GCCCCTGAGT CTCCACCTGG CTGCTGGCAG CCCCACAGGG AGGTTCGGCG AAACTGAGGC 480
TTGCCAAAGA AGCCTTTGTC CAGAGTCACG CAGCTGGCGC GGTGGAGCCA GGGCCAGAAC 540
CCGTGCAGGC TGATCCCAGC CTGCCTTCTC CACTGTGCCC CGAGGACCAC TTTCTTTCCT 600
GGGAGTGTGT GTGTGCACAT GTGCTGTGTC CTGTCGTCTG TACACACTTG TGCCTGGCGT 660
GAGGCAGGAT GTCTGGCTGG ATCTACCAGA AAGTATTCAC AGCGGGTTCT CCAGCTGGGG 720
TGAGGGGCTT GGGCTCGCAG GGAGGGAGCC TACTTTTCAC TTTAGCTTGC TTTCTTCCTT 780
TCTTCCGTCC TTCCTTCCTC CCTCCCTCCC CTCCCCTTCC CACCCCTTCT TTCTCTTTCT 840
TCTTTCTCTT TCTTTCTTTC TTTCCTTCCT TCCTTCTTTC CTTTCTCTTT CTCTTTTTTT 900
CTTTCTTCCC CTTCCTTCCT TCCTTTCTTG TTTTTGTTTG TTTGTTTGAG ACAGGGTCTC 960
ACTCTGGTAT GCAGGCTGGA GTGCAGTGAT GCAATCATAG CTCACTGCAG TCTCCTGCAG 1020
AACTCCTGGG CTCAAGCGAT CCTCCCACCT CAGCCTCCCA AAGTGCTGGG ATTACAGGCA 1080
TGAGCCACTG TTCCTGGCTT ATTTGTGTTT TCTTTTTTTT TTTTTTTTTT TTTTTTTTGA 1140
GACGGAGTCT 1150