EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS187-16540 
Organism
Homo sapiens 
Tissue/cell
Th1 
Coordinate
chr22:50337900-50339980 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GCM1MA0646.1chr22:50338288-50338299CATGCGGGTAC+6.62
ZfxMA0146.2chr22:50338091-50338105CAGGCCTCAGCCCC-6.21
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_10057chr22:50337764-50339995CD14
SE_10530chr22:50338223-50338749CD19_Primary
SE_10530chr22:50338855-50340155CD19_Primary
SE_11301chr22:50337371-50340370CD20
SE_12420chr22:50338129-50340096CD3
SE_17545chr22:50337358-50341301CD4p_CD25-_CD45RAp_Naive
SE_17909chr22:50337253-50340777CD4p_CD25-_CD45ROp_Memory
SE_23129chr22:50337861-50338538Colon_Crypt_1
SE_23129chr22:50339336-50339949Colon_Crypt_1
SE_23738chr22:50337894-50338535Colon_Crypt_2
SE_23738chr22:50339474-50339920Colon_Crypt_2
SE_24687chr22:50337135-50338557Colon_Crypt_3
SE_24687chr22:50339454-50339903Colon_Crypt_3
SE_31381chr22:50336439-50338682Gastric
SE_31381chr22:50338853-50339966Gastric
SE_34375chr22:50337498-50340123HCT-116
SE_35007chr22:50337640-50340278HeLa
SE_41617chr22:50339456-50339853LNCaP
SE_42159chr22:50337434-50338605Lung
SE_47471chr22:50339107-50339443Pancreas
SE_47471chr22:50339517-50339940Pancreas
SE_50117chr22:50337730-50338610Sigmoid_Colon
SE_50117chr22:50339205-50347666Sigmoid_Colon
SE_52469chr22:50337748-50338591Small_Intestine
SE_52469chr22:50338933-50339975Small_Intestine
SE_53398chr22:50337357-50338476Spleen
SE_53398chr22:50338967-50339914Spleen
SE_61206chr22:50315437-50364432HBL1
SE_61985chr22:50315627-50364432Toledo
SE_62450chr22:50318672-50364388Tonsil
SE_68380chr22:50327316-50364640TC32
SE_68381chr22:50327316-50364640TC32
SE_68382chr22:50327316-50364640TC32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr225033847350339938
chr225033898650339884
chr225033880550338926
chr225033802650338636
Number: 1             
IDChromosomeStartEnd
GH22I049942chr225033615950349619
Enhancer Sequence
TGTGGGCCCG AAAGGGATGG GGAGGCTCCT GCTCATCCTC AGCTGCACTC CCGCCCCCAC 60
TGCCCCTCTG GGAAGCCCCT GGCGTCTAAC GTCCCATCAG CCAAAGACTT GCCAAGCACA 120
GGCCCAGGCC TGGTCACCCC CAGCAGGGTC ACCTCACTCT GGCCATGGAG GAGGTTGTGA 180
CACAGGATGG CCAGGCCTCA GCCCCACAGA GCTGCCTCCC TGAACCCTGT CCTGGCCTGG 240
GAAGACTGGC TCTCACACTG CTGGGCCTGG GGACCAAGCC TGTGGGCAGA AGCGGCCCTC 300
CAACGCTCAG GACAGGCCTG GGGTTGTCCA GGCCTCCCGG GTCCTGCCTC CTCCTGGACC 360
TGGCCTTGGT CTGAGCACCT GTTCTCTCCA TGCGGGTACC TGGGCCTCTG AAATCCCCGC 420
TGGTGGAGGA GGTGTTGGGT GGCCCAGGAT CACCAGCACA CCAGGTGGCA GCCTCCACCC 480
CAGACCTCAG GCTGCAGTGC CAGGCACCCA GAGCGCCAGG AGCCCACCGC AGTCACAGTG 540
ACAGCCGGGC CGTGCATCTT GGGGTGCGCT TGCGCCAGCC CAGAGCTCCT GACCGCATGA 600
TGTCCTGGGG GGTTGGGACC CGGAAAAAAG TCTCACTGCT CACCAGCCCC CCAGGAAACT 660
CCGCCCCTTT ACAGTGTCGC TGCTCACCAG TACCCCCAGG AAACTCTACG CCCCTTTACA 720
GTGTCACTGC TCACCAGGTC CCCCAGGAAA CTCTACGCCC CTTTACAGTG TCACTGCTCA 780
CCAGGTCCCC CAGGAAACTC TACGCCCCTT TACAGTGTCA ACTGCTCACC AGGTCCCCCA 840
GGAAACTCTA CGCCCCTTTA CAGTGTCACT GCTCACCAGG TCCCCCAGGA AACTCTACGC 900
CCCTTTACAG TGTCACTGCT CACCAGGTCC CCCAGGAAAC TCTACGACCC TTTACAGTGT 960
CACTGATCAC CAGGTCCCCC AGGAAACTCC GCCCCTTTAC AGTGTCACTG CTCACCAGCC 1020
CCCCAGGAAA CTCCGCCCCT TTACAGTGTC ACTGCTCACC AGCCCCCCAG GAAACTCCGC 1080
CCCTTTACAG TGTCACTGCT CACCAGCCCC CCAGGAAACT CTGCCCCTTT ACAGTGTCAC 1140
TGCTCACCAG TCCCCCCAGG AAACTCTGCC CCTTTACAGT GTCACTGCTC ACCAGGTCCC 1200
CCAGGAAACT CCGCCCCTTT ACAGTGTCGC TGCTCACCAG CCCCCCCCAG GAAACTCCGC 1260
CCCTTTACAG TATTGCTGCT CACCAGCCCC CCAGGAAACT CCGCCCCTTT ACAGTGTCGC 1320
TGCTCACCAG CCCCCCCAGG AAACTCCGCC CCTTTACAGT GTTGCTGCTC ACCAGTCCCC 1380
CCCAGGAAAC TCCGCCCCTT TACAGTGTCG CTGCTCACCA GCCCCCCAGG AAACTCCGCC 1440
CCTTTACAGT GTCACTGCTC ACCAGCCCCC CAGGAAACTC CGCCCCTTTT GGGGCCAGAG 1500
ATGCTGTGAG AAGTGGCCTT TTATTATATA AAACTGTTTT ATGCAGAATT TAAGATGTAC 1560
ATGTGACCCC TGAGATTAAA CCACAGCCCC AAACAGCTCC CTGATTTTAG CCTTGTAGGA 1620
GACCCTGGGG CAGAGGGAAA CTGCTAAACC AGACTTGGAT TCCAGACCCA CCTGGAAGTC 1680
ATAAATGTGT GTTGTTTTAA GCCACTATAA TTTGGAGTCG TTTGTGACAC AGCAGAGCAA 1740
CAGATTACCA TCATGGTGTT GAAGGTAGAG CCAGCTGGGC TTGCTGGCTG ACTCCAGGGC 1800
ATTGGAGGAC GCCAGAGCAT TGACCTGAGC CCCTGGCAGG TGTGGCTGGC AGCATTGGGA 1860
CAAGGACAAC GAAGGCTGCA AGTCAAGAAC TCTGCGCTGG GGCCAGGCGG CGGCTCACAC 1920
CTGCAATCCC AGCACTGTGG GAGGCTGAGC CTGATGGATC ACCTGAGGTC AGGTTTGAGT 1980
TCAGCCTGCC CAACATGGTG AAACCCCGTC TCTACTAAAA ATACAAAAAT TAGCCAGGCA 2040
TTGTGGTGCA TTCCTGTAAT CCCAGCTACT CAGGAGGCTG 2080