EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS111-03435 
Organism
Homo sapiens 
Tissue/cell
KB 
Coordinate
chr22:50326880-50329270 
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ArMA0007.3chr22:50326959-50326976AGGAACATGCTGTTCTA+6.21
E2F6MA0471.1chr22:50329019-50329030GGGCGGGAAGG+6.62
FOSL2MA0478.1chr22:50328189-50328200GGGTGACTCAG+6.02
JUNBMA0490.1chr22:50328189-50328200GGGTGACTCAG+6.02
Klf1MA0493.1chr22:50328039-50328050AGGGTGTGGCC-6.32
NR3C1MA0113.3chr22:50326959-50326976AGGAACATGCTGTTCTA-6.01
NR3C1MA0113.3chr22:50326959-50326976AGGAACATGCTGTTCTA+6.1
TCF3MA0522.2chr22:50329211-50329221AGCAGGTGTT-6.02
ZNF263MA0528.1chr22:50329123-50329144CGAGGAGGTGGGGGGAGGGGA+6.07
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_03028chr22:50328039-50328938Bladder
SE_10057chr22:50326655-50329475CD14
SE_10530chr22:50326533-50329357CD19_Primary
SE_11301chr22:50322859-50332155CD20
SE_12420chr22:50327597-50329064CD3
SE_17545chr22:50326591-50331700CD4p_CD25-_CD45RAp_Naive
SE_17909chr22:50326643-50331570CD4p_CD25-_CD45ROp_Memory
SE_23129chr22:50326762-50329014Colon_Crypt_1
SE_23738chr22:50326901-50330921Colon_Crypt_2
SE_24687chr22:50326851-50332818Colon_Crypt_3
SE_26808chr22:50326694-50332325Esophagus
SE_28169chr22:50328251-50328925Fetal_Intestine
SE_31381chr22:50326539-50332985Gastric
SE_34375chr22:50326902-50329045HCT-116
SE_35007chr22:50326543-50329240HeLa
SE_42159chr22:50326486-50329239Lung
SE_47471chr22:50327181-50329026Pancreas
SE_49712chr22:50326718-50329026Right_Ventricle
SE_50117chr22:50326592-50329123Sigmoid_Colon
SE_52469chr22:50326640-50328989Small_Intestine
SE_53398chr22:50326561-50333542Spleen
SE_56937chr22:50327618-50330661VACO_400
SE_61206chr22:50315437-50364432HBL1
SE_61985chr22:50315627-50364432Toledo
SE_62450chr22:50318672-50364388Tonsil
SE_65335chr22:50326556-50329404Pancreatic_islets
SE_68380chr22:50327316-50364640TC32
SE_68381chr22:50327316-50364640TC32
SE_68382chr22:50327316-50364640TC32
SE_69071chr22:50328213-50329028H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr225032844250328844
chr225032765250328200
chr225032773050328489
chr225032721350327243
Enhancer Sequence
GACCTCCGCA TCACACAACC CTAATATATT TTGCTCCAAC AAGCTGAGCA GTCTCTTGTG 60
GGCTGCCTGT CCCTCTCCCA GGAACATGCT GTTCTATCAG CCACCTCCAC AACCCCACGC 120
AGCTCTGACC CTGGGCCCGC TCCAGCCCTG CAACTCATTA GAGAGCTGCC TTCACAGCCA 180
CTGATGGTCA AATGCTGCTG CCTGGCCATC ACCCCCGTCC CTGTCAGCCA GTCCAGTGCT 240
GTGACCGTCC CCTGCTCTCA GTTCCAGAGG ACAGCTGGGA TCTGTGGTGC CACATGACTT 300
TCAGCCCCTG TCTGCGGTGG CTGTTCTGAC ATTCACCCCT CCTCACGTGT GTCCCACACT 360
CCAGGAGCCT CTGGGCCGTG AAACAGAGCA GCAGAGGACA CCGCCTCCTG GGGTCCTAGT 420
CCTCAGAAAA GGGCCCACAA CCCGTCAGCT CTCCGCCGTC CACCACATGC AGCTTATCTG 480
GCTGGGCACG GCTTCGGGTC CCGGGCTCCT TCAGGCTGTG GCCCCTTTGT CACTGGGCCA 540
GCACATCCCC ACCAGGATAC ACTGCAACTT AATCCCAGGA GGGTCTCGGG CAGGTCCTGG 600
GTAATCCCAG GAGGGTCTCG GGCAGGTCCT GGGGAGCCGG GGCAGGGGGC CGGCCTCTCC 660
CACGGAGGAG GCACGGTTTG GAGACATCCT GTTTCTTCCC AGCCAGCACC GAGGCCGGGG 720
CACAGCAGAC CCCCGGGGAT GGGGTCACCT ATTGGTGGCC CCTCTGGTCA CTGAGTCTGT 780
GCGTGTTCTC CTGGCCTCTC CATGCAGCCT TCTGTTGTTT TTCCAGAGCT TCAGGGGCGG 840
GCACCAGCAG CCCCCCGAGG ACACTGTTCT CAAGGTTGTG CCCCCTGGAC TCTCACCCCA 900
GGCTCACCCA CCCCAAGAGT GCAGGCCCCT TCCCGTCGCG TCCACCGCCA GTGGTGCCCG 960
CTGGACAGAG TGCCTTTGCC TGTACACCTC CCTGGCGCTG CCTGTCTGTG GCTGGCTCCA 1020
GAGTGGCAGG CGGTCTTGGC GCCTCAGCCA TGTCCTCAGC TGACCTGGGG GCTGGGTGAG 1080
GTGAGGCACC CTGAGACTTC TTCAGCGTGC TGAGCTGTGA GGAGGGGGCT GGGCCTTTGG 1140
CCACCACAGG ATGACTCAAA GGGTGTGGCC TTCAGTGGGG TGCTCTCCTC AGCCTGCCCC 1200
TGCTGCTCCC TCAGCCCCCC GGTCCGGCTC TGTCCCTTTT CAGACTCCCA GACCCCGCAG 1260
GCCTGGGGTG GGGACTCTGC CTGCCACCTG GGAAGGGTGG TCGTCAGTGG GGTGACTCAG 1320
GGTGGAGGGC CCTGGCCCAG TGGCCCTGCC CTCCTCCTCA TATGCCCGTG ACCAGCACGC 1380
GGGTGTGGAC TGAGCCTGTG CCAGGTGGGC CCTGGGGGTC GGGGGGCAGA AGGGCCCAGG 1440
TCCTGCAGGG GAGTGGGGGG CGGTGCTGGG GCCCAGAAAG GCTTACTGTA ATGTGGCTGG 1500
TGGGGGCCAC CGGCTCTCAG GCCACACACT CCCCCTCCAG GCCCAGCGCC CCTCCCCGCC 1560
TCCCTGGGGC TGCGGTCTTC CCAAACCCCA AGCCGGCTGC TCTGCACCAG TGAGGGGCCG 1620
GGAGTGGCCT GGCCTGAGGA GGCTGCAGGG CACCCACCTC TCCAGAGACC CCCTCCACCC 1680
ACTCCCGGGG GATCCTTCTG GAGAGACCGT TCCCAGCCGT TGAGCAGGGT CCGCTCTCCC 1740
CCCTACCCCG GTCTGGCCTT TGGGAGGATC CCCCCAGAGC CAGGGAGGGG TATCTGGCCC 1800
CTCACCCCTC AAACGGCAGT CCAGGGCCAG CGTCTTTCTG CGCTCACCCA CCTGCCTGCG 1860
ACGGGGCTCT CTGGGCCACA GGGCGGCCAC CACTCGAGGG TCACCCGCAA GCCTCGGAGT 1920
CCCTGCTCGG AGCGGGGGCT GGTGGTCGCG GTGGGGGTGG GGAGCGGGCA CCCACTGGGG 1980
ATTCACCCCA CCCGGGCCCC CCTCCAGCCT CTGCCCGGCG CCCGGGTCTT CGGTCCGCCC 2040
TTTGCAGAGG AAGGACCCCG CCCTGCGCAG AGCGGGCTTG GGGGACCCGG GCGGGCGGCG 2100
GGGCGCGGGG TGGGGCGCGG GGGGCGGTGT TGCTCCCGCG GGCGGGAAGG GCGGGGAGCG 2160
GCCCTGCCGG GAAGGGGGCG GTGCCGGAAG CGTCAGCTGG GCTTTCCCCG GCGGGCGGGG 2220
GCGGGGAGCA GATGGGGGCG CTACGAGGAG GTGGGGGGAG GGGACGCAAT GGAGGTGCCG 2280
GGGGTGCGCT GAAGAGCGAG ACTGGGGCAG GGGGATGAGG GTCTGGGAAG GAGCAGGTGT 2340
TGGGGACGGA GGGTGGGGGC GGGGAGTGGG GGCGCGGGGA GGAGCAGGGT 2390