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

TagContent
EnhancerAtlas ID
HS170-02564 
Organism
Homo sapiens 
Tissue/cell
RS4-11 
Coordinate
chr22:30700830-30703700 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Stat6MA0520.1chr22:30701600-30701615GGTTCTCAGGAACAG-6.5
ZNF143MA0088.2chr22:30702100-30702116CACCTATAATGCACTG+6.12
Number of super-enhancer constituents: 32             
IDCoordinateTissue/cell
SE_00207chr22:30696033-30714616Adipose_Nuclei
SE_01017chr22:30700143-30702296Adrenal_Gland
SE_01017chr22:30703060-30703633Adrenal_Gland
SE_01933chr22:30698201-30702501Aorta
SE_03076chr22:30699977-30702532Bladder
SE_06187chr22:30696247-30703814Brain_Hippocampus_Middle
SE_11435chr22:30693586-30712890CD20
SE_12307chr22:30699489-30707598CD3
SE_15119chr22:30696526-30703994CD4_Memory_Primary_7pool
SE_16208chr22:30700645-30707378CD4_Naive_Primary_7pool
SE_18199chr22:30696796-30709288CD4p_CD25-_CD45ROp_Memory
SE_19840chr22:30699216-30703747CD4p_CD25-_Il17p_PMAstim_Th17
SE_22773chr22:30696696-30709496CD8_primiary
SE_23721chr22:30699936-30702628Colon_Crypt_1
SE_25730chr22:30696761-30709491DND41
SE_26571chr22:30696437-30709562Esophagus
SE_31521chr22:30697029-30703752Gastric
SE_34216chr22:30697102-30703879HCC1954
SE_39484chr22:30699161-30703889Jurkat
SE_41271chr22:30696285-30703529Left_Ventricle
SE_41665chr22:30699347-30702386LNCaP
SE_41665chr22:30703002-30703645LNCaP
SE_42270chr22:30696389-30702599Lung
SE_42270chr22:30702620-30703740Lung
SE_47736chr22:30701092-30701830Pancreas
SE_48841chr22:30699273-30702488Right_Atrium
SE_50213chr22:30696873-30703874Sigmoid_Colon
SE_53095chr22:30699170-30702601Small_Intestine
SE_53095chr22:30702643-30703768Small_Intestine
SE_55187chr22:30700198-30703764Thymus
SE_63164chr22:30696999-30708171Tonsil
SE_66498chr22:30699161-30703889Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr223070200030702541
chr223070245330702564
chr223070120030702000
Number: 1             
IDChromosomeStartEnd
GH22I030300chr223069653430717414
Enhancer Sequence
AGCAGGTGGT TCAAGTGCCT ACTTCCCTAA TGTGGCCAGG ACCCATGGTA CCTCTCTGAG 60
GCAGAGGCTG AGTGAGTGTC TGCATCTGTG CAGCAAAGCA AAGCATTCCT GTCCTGGGTC 120
TGCCTTAGTC AATAAGCCTC TTCAGAGGGC CGGTGTACAA GGTGCAGAGT TGAACACAAA 180
AACTAGTCAA ACGAGTACAG AAATAATATG CTCACCTCTT TACTTGAGCC AAACTCATTA 240
CTCAGAGTTT CCCCAATTAT GCCCTGGCCC TTTCCCTCTC AGCCTTTATT CATGCCAGTA 300
ACTTTGCTGG AATGCTTCCC AAATCGTCTC CACCCATCAA AATCCTACAC ACACTTCAAA 360
GCCCCATCAA ATACCACTTC TTCTATCTGT AGATCTACTG ACTGGGCAGC TAGCACAACT 420
GTGTTGCAGT GTTCTAGGGC GAGGGCCTCT GGATGGGTTA TGGGGATGCC GTCCCATGAT 480
TAAAACAAAG TCTTGACCCT CATGGAGTTG ATATTCTGGT GGGCACTGAA TGTGGGGAAA 540
ACACCTCAGC ACCAAGGTGC TTTTTTCTGC TTTCTTAACA GAATAAGGTA TTAATGACAG 600
ACAAGGAAAC AGGCTTAGAG AGGTAAGATA CTCAGGAAAG GTATCTTGCT TAGCGTTCAA 660
TCAGTGGAAA AACCCAGACT CAAATACAAG TCAGGTCCCA GCCAAGAGCC AGCACACAGT 720
GCTGCCTGAC CTCTCAGAAA GGAGCACAGA GTCGGAGGCA GCTCAGAGGA GGTTCTCAGG 780
AACAGGACAC AGTGGGGCTG GGGCTTGGCC CAGGCCTGAG TCTCTGATCC TCTCTCTGCC 840
GGAAGGAAAT GTGCTACTGT GACTTTTACT GGTTGGAAGA GCAGAGGGAG GGGCCCTGGC 900
AGAGCTGAGG CCTCTAAGAC ACAAAAGGGA AGGTCTTCTT CAGTGCATTT TATCTGGGGA 960
AGTGCCCAGG CCTGAGAGTA GCCTTGGAAC TGAACGTCTG AGGAAGGACT ACAGCCCAGG 1020
CAAAGGAGGC CCCCTCAACG CACTGATACA AGGCACCCCA CCTTGAACTG CTGCCCCTCT 1080
CACCACCTAA AGGCAGAACT AGGGCATGAG TTACTCCTTT CTTTGCCTTT CCTGATAAAA 1140
GCAAAGCAAG GACCACGCCT TTACAAAAGG TCAGGTAATT TACAAAGGGA TATGTATCTC 1200
CGGGCAACCC CCAAACATCC CAGGAGCAGA AACTAAGGGC CCACACCTCC CAGGCCATGA 1260
TACCTTCCAC CACCTATAAT GCACTGCTTA TGCAACAAGT CAGAGGAACA GCCTTCTAGT 1320
TAACCAGTCA GAAGGGTGCC CAAACTGAGT CAACAGGAAG TTCTGGCAGT TATGGATGTA 1380
GATAATGGCT AATCCAATAT CCCCACTGCA CAGATGAAGA AACTGAGGCT TACAGAGGGC 1440
AAGGTTTTCA CTTGAGATTA CCAGTTTCCA AAGAACTCAC AGGTGATTAA ATATGTCTAT 1500
CTGATACCTC AACCCTCAGT CTGGCTTTAT TGATAAAATC TAACTGCAGG GACTCAAAGA 1560
TGCCCATTCT CCCAACTGCA GATACACAGA GGAACATGTT AAATTCAGAG TTCTTTTAAC 1620
TGATGCCAGA TAACAGCTTT GGCAGTTTCA AACCCCCAAT GTCAAACCTC AAACCGGAAC 1680
TTCAGAAGAG TACAAAACAA ACTACCATAT TTCCTGGATT CTAAGACACC ACTGATTTTA 1740
AGCTACACCA TTGATTTGGC AAGATCTTCT CAGAAACAAA CAAAAAACCC ACTACTACTT 1800
TAACTGTGCA TGTCAATTGA AAGATCTGTT TTGATTTTTT AAATCCTAAA TTAGGAAAAT 1860
TTTAAGGCAA TATGGCCATC TGAATGGCTT TTCCTTTAAC AGCAGAGGAG TTTAATCTAC 1920
CTGGAGATGG TGAGAAGGAA GACACTGGAG GTCTGGCTGT ACCCAGCACT CAGCGTACCA 1980
CATGCTCTCT AACTGCAGGT AGATGTCTCT AGGCACAGGA TATACTCCTG AAACATTGCA 2040
GGCTATCTAT TTTTTTTGTT GTTAAATCAG AAGAGTCACA TATCCTTCAA TTAACTCAGT 2100
CAGGATCTTA GAAAACATCT GATCCAACTG CTGTCTGATA TAGAAATCCT TTCTACATTA 2160
GGCAAGTCCC CTTTCTTCTC TGATCCTCAG TTTCGCTATA TGCTTGTACA GTCTATCTTA 2220
TGAATTTGAC CCTCTAAGGA GGCCCACAGA GGAGCTGTGG GATGAAGCTG GGGCCAGAGG 2280
GGTCCCTGAA AATAGTATGA CAGTGTAGAA GCCCTGAGGA GGCTTCCTCC TGACAGTGGA 2340
GAGGGCAGGA ACCAATTGCT AGTGAGAGAG AAGCTGGCCC AGTATAAGGG ACCACAAATG 2400
GCCCATGGGG GATGTCGCAA ATCTGGCGGC CTCACTCATC CTCCAGAAAA CCCCTCCTTC 2460
CTTAAGGTAG ACTGAGGGAG TCTCTGAAGC CAAAAGAGAC AAGTGAGACC AGTTTCTTTT 2520
GGCTCAGCCA CTGCTGGAAC TCCTCCAGGG ATGGGCCTTC CTTACCTCCA GGTGAAGTCA 2580
CTCTATTGTT AAACAGTTTC CACTGCTAAA GCTTTCTTCC CCACCTTATG CCAAAATTGT 2640
CCTAGTAACT TCCACCGTAA TCTCAACACC GCTTTTGAGG CCATACAATT CTCCCATACC 2700
AGGCACACAC ATGTTTATCC CTCACCATCC ACTCATCCCT AACTGAATGC CCTTTCTTCT 2760
CCCTTCTCCA AGTGACAGTA ACCCTTCAGA GCCCAATATT ACATTAAAAA CCATCACTAC 2820
AACAATAATA ATATCAGCAA CAGTAGTTAC CATTCGTAGA TTATTTACTA 2870