EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS149-00844 
Organism
Homo sapiens 
Tissue/cell
NKC 
Coordinate
chr22:50326600-50329430 
TF binding sites/motifs
Number: 10             
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
ZNF263MA0528.1chr22:50329352-50329373GGAGGCGGAGGGGAGGGTGGG+6.62
Number of super-enhancer constituents: 31             
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_23129chr22:50329041-50330887Colon_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
GAGTGCGGTG GTGTGATCTC AGGTCACTGC AACCTCTGTC TCCCAGGTTT AAGCAATTCT 60
CCTGCCTCAG CCTCCCGAGT AGCTGAGATT ACAGGCACCT GCCACCACGC CCAGCTAACT 120
GTTGTATTTT TAGTAGAGAT GGGGTTTCAC TATGTTGAGC AGGCTGCTCT TGAACTCCCG 180
ACCTCAAAGT GATCCACCTG CCTTGGCCTC GCAGAGTGCT GGGATTACAG GCTTGAGCCA 240
CCACGACCGG CCCTGACTTT TTATTGGAGC GAGTACCCTT GACCTCCGCA TCACACAACC 300
CTAATATATT TTGCTCCAAC AAGCTGAGCA GTCTCTTGTG GGCTGCCTGT CCCTCTCCCA 360
GGAACATGCT GTTCTATCAG CCACCTCCAC AACCCCACGC AGCTCTGACC CTGGGCCCGC 420
TCCAGCCCTG CAACTCATTA GAGAGCTGCC TTCACAGCCA CTGATGGTCA AATGCTGCTG 480
CCTGGCCATC ACCCCCGTCC CTGTCAGCCA GTCCAGTGCT GTGACCGTCC CCTGCTCTCA 540
GTTCCAGAGG ACAGCTGGGA TCTGTGGTGC CACATGACTT TCAGCCCCTG TCTGCGGTGG 600
CTGTTCTGAC ATTCACCCCT CCTCACGTGT GTCCCACACT CCAGGAGCCT CTGGGCCGTG 660
AAACAGAGCA GCAGAGGACA CCGCCTCCTG GGGTCCTAGT CCTCAGAAAA GGGCCCACAA 720
CCCGTCAGCT CTCCGCCGTC CACCACATGC AGCTTATCTG GCTGGGCACG GCTTCGGGTC 780
CCGGGCTCCT TCAGGCTGTG GCCCCTTTGT CACTGGGCCA GCACATCCCC ACCAGGATAC 840
ACTGCAACTT AATCCCAGGA GGGTCTCGGG CAGGTCCTGG GTAATCCCAG GAGGGTCTCG 900
GGCAGGTCCT GGGGAGCCGG GGCAGGGGGC CGGCCTCTCC CACGGAGGAG GCACGGTTTG 960
GAGACATCCT GTTTCTTCCC AGCCAGCACC GAGGCCGGGG CACAGCAGAC CCCCGGGGAT 1020
GGGGTCACCT ATTGGTGGCC CCTCTGGTCA CTGAGTCTGT GCGTGTTCTC CTGGCCTCTC 1080
CATGCAGCCT TCTGTTGTTT TTCCAGAGCT TCAGGGGCGG GCACCAGCAG CCCCCCGAGG 1140
ACACTGTTCT CAAGGTTGTG CCCCCTGGAC TCTCACCCCA GGCTCACCCA CCCCAAGAGT 1200
GCAGGCCCCT TCCCGTCGCG TCCACCGCCA GTGGTGCCCG CTGGACAGAG TGCCTTTGCC 1260
TGTACACCTC CCTGGCGCTG CCTGTCTGTG GCTGGCTCCA GAGTGGCAGG CGGTCTTGGC 1320
GCCTCAGCCA TGTCCTCAGC TGACCTGGGG GCTGGGTGAG GTGAGGCACC CTGAGACTTC 1380
TTCAGCGTGC TGAGCTGTGA GGAGGGGGCT GGGCCTTTGG CCACCACAGG ATGACTCAAA 1440
GGGTGTGGCC TTCAGTGGGG TGCTCTCCTC AGCCTGCCCC TGCTGCTCCC TCAGCCCCCC 1500
GGTCCGGCTC TGTCCCTTTT CAGACTCCCA GACCCCGCAG GCCTGGGGTG GGGACTCTGC 1560
CTGCCACCTG GGAAGGGTGG TCGTCAGTGG GGTGACTCAG GGTGGAGGGC CCTGGCCCAG 1620
TGGCCCTGCC CTCCTCCTCA TATGCCCGTG ACCAGCACGC GGGTGTGGAC TGAGCCTGTG 1680
CCAGGTGGGC CCTGGGGGTC GGGGGGCAGA AGGGCCCAGG TCCTGCAGGG GAGTGGGGGG 1740
CGGTGCTGGG GCCCAGAAAG GCTTACTGTA ATGTGGCTGG TGGGGGCCAC CGGCTCTCAG 1800
GCCACACACT CCCCCTCCAG GCCCAGCGCC CCTCCCCGCC TCCCTGGGGC TGCGGTCTTC 1860
CCAAACCCCA AGCCGGCTGC TCTGCACCAG TGAGGGGCCG GGAGTGGCCT GGCCTGAGGA 1920
GGCTGCAGGG CACCCACCTC TCCAGAGACC CCCTCCACCC ACTCCCGGGG GATCCTTCTG 1980
GAGAGACCGT TCCCAGCCGT TGAGCAGGGT CCGCTCTCCC CCCTACCCCG GTCTGGCCTT 2040
TGGGAGGATC CCCCCAGAGC CAGGGAGGGG TATCTGGCCC CTCACCCCTC AAACGGCAGT 2100
CCAGGGCCAG CGTCTTTCTG CGCTCACCCA CCTGCCTGCG ACGGGGCTCT CTGGGCCACA 2160
GGGCGGCCAC CACTCGAGGG TCACCCGCAA GCCTCGGAGT CCCTGCTCGG AGCGGGGGCT 2220
GGTGGTCGCG GTGGGGGTGG GGAGCGGGCA CCCACTGGGG ATTCACCCCA CCCGGGCCCC 2280
CCTCCAGCCT CTGCCCGGCG CCCGGGTCTT CGGTCCGCCC TTTGCAGAGG AAGGACCCCG 2340
CCCTGCGCAG AGCGGGCTTG GGGGACCCGG GCGGGCGGCG GGGCGCGGGG TGGGGCGCGG 2400
GGGGCGGTGT TGCTCCCGCG GGCGGGAAGG GCGGGGAGCG GCCCTGCCGG GAAGGGGGCG 2460
GTGCCGGAAG CGTCAGCTGG GCTTTCCCCG GCGGGCGGGG GCGGGGAGCA GATGGGGGCG 2520
CTACGAGGAG GTGGGGGGAG GGGACGCAAT GGAGGTGCCG GGGGTGCGCT GAAGAGCGAG 2580
ACTGGGGCAG GGGGATGAGG GTCTGGGAAG GAGCAGGTGT TGGGGACGGA GGGTGGGGGC 2640
GGGGAGTGGG GGCGCGGGGA GGAGCAGGGT GGGGGCGGAG GGGAGGATGG GGGTCCGGGA 2700
GGAGCAGGGG CGGGGACGGA GGGGAGGGTG GGGGTCCGGG AGGAGCAGGA GTGGAGGCGG 2760
AGGGGAGGGT GGGGATGTGG GAGGAGCAGG GGTGGGGCAA AGGGGAGGGT GGGGGGTTCA 2820
GGATGAGCAG 2830