EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS102-15191 
Organism
Homo sapiens 
Tissue/cell
HuCCT1 
Coordinate
chr22:30697340-30699880 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NFIAMA0670.1chr22:30697797-30697807GGTGCCAAGT+6.02
RUNX1MA0002.2chr22:30698223-30698234AAACCACAGAG-6.14
SPI1MA0080.4chr22:30698742-30698756GAAAAGGGGAAGTG+6.64
SPIBMA0081.2chr22:30698744-30698756AAAGGGGAAGTG+6.07
ZBTB18MA0698.1chr22:30697363-30697376GAACATCTGGATG-7.82
ZNF263MA0528.1chr22:30697829-30697850AAAGGAGGCAGAGGAAGGGGG+6.86
Number of super-enhancer constituents: 39             
IDCoordinateTissue/cell
SE_00207chr22:30696033-30714616Adipose_Nuclei
SE_01017chr22:30697528-30699059Adrenal_Gland
SE_01933chr22:30698201-30702501Aorta
SE_03076chr22:30697273-30698942Bladder
SE_06187chr22:30696247-30703814Brain_Hippocampus_Middle
SE_11435chr22:30693586-30712890CD20
SE_12307chr22:30697444-30699157CD3
SE_12307chr22:30699489-30707598CD3
SE_15119chr22:30696526-30703994CD4_Memory_Primary_7pool
SE_16208chr22:30697107-30699229CD4_Naive_Primary_7pool
SE_18199chr22:30696796-30709288CD4p_CD25-_CD45ROp_Memory
SE_19840chr22:30697181-30699157CD4p_CD25-_Il17p_PMAstim_Th17
SE_19840chr22:30699216-30703747CD4p_CD25-_Il17p_PMAstim_Th17
SE_22773chr22:30696696-30709496CD8_primiary
SE_23721chr22:30697471-30699113Colon_Crypt_1
SE_23721chr22:30699316-30699931Colon_Crypt_1
SE_25730chr22:30696761-30709491DND41
SE_26571chr22:30696437-30709562Esophagus
SE_31521chr22:30697029-30703752Gastric
SE_34216chr22:30697102-30703879HCC1954
SE_39484chr22:30697242-30699103Jurkat
SE_39484chr22:30699161-30703889Jurkat
SE_41271chr22:30696285-30703529Left_Ventricle
SE_41665chr22:30697626-30698975LNCaP
SE_41665chr22:30699347-30702386LNCaP
SE_42270chr22:30696389-30702599Lung
SE_47044chr22:30697038-30698916Ovary
SE_47736chr22:30697890-30698326Pancreas
SE_47736chr22:30698345-30698991Pancreas
SE_48841chr22:30696485-30699248Right_Atrium
SE_48841chr22:30699273-30702488Right_Atrium
SE_50213chr22:30696873-30703874Sigmoid_Colon
SE_53095chr22:30697322-30699159Small_Intestine
SE_53095chr22:30699170-30702601Small_Intestine
SE_55187chr22:30697421-30699335Thymus
SE_55187chr22:30699338-30700146Thymus
SE_63164chr22:30696999-30708171Tonsil
SE_66498chr22:30697242-30699103Jurkat
SE_66498chr22:30699161-30703889Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr223069804930698990
Number: 1             
IDChromosomeStartEnd
GH22I030300chr223069653430717414
Enhancer Sequence
GATGGGCGCT CGGGGCATGA GAAGAACATC TGGATGTGGG TTTGAATCTA GCGCTGACCT 60
TAAGCCAACC ACTTCTCAAC TGTAAGATCT GAATAATACC TACTACTGTG CAGAGTTGTC 120
AAAGGAGTCC ATTAGAGAGG GAAAATGTGC TTAGTGTGGG GCCTGACACA GTCTGTGTTC 180
AGTAAGCAAT GGCTTCCTCT CTGCCCCTCC ATCCCAGGAG GATGCTTGAC ACAGAAGCCC 240
AGGACCTCAG CTCACACCTA ACTTCCCCTC ACCTAGAAAC CCCCTTCAAC AGTCCTGCTG 300
GAAGCTCTCA GAGGAGGGAG TACAGAAGCC CTGGCCTTCC TGGGGACCAG TGCAAACAAG 360
AGAAAACTTT CCAAGGGTCA GAGAGAGTCA AGAACCAGGA AGGAGCCAGG CAAACAGGCT 420
GAGGGTGGTG GGGGAAGAGT AGCAGTGGCT GGTCACAGGT GCCAAGTGAG AGCTTCTGGG 480
ACTGCCTAGA AAGGAGGCAG AGGAAGGGGG CTGAAGGGAA CTGCACTAGA CGCAAGGAAG 540
AGTTTCCTGC GGCTATGGGA CAAGGGTCTC CTTAAGGAAG CCAACTTGGG CAGGCTTTGG 600
CAAAGGGATG TGCTTTAGCC CAAAGCCACA GGCCCTTCAG GCTCTCCCAC AGAGCTAAGC 660
TCAGCAAGAG GCAGCCCCAC ATCATCACAG CCCCCATCAT ATTTGGCCTT CTCCAGGAGA 720
GCCCTGGAAC ACTTCGCGGG CAGCAAAGAG CTGGGAGTAC AGCCAGCCTT TCCCACTCTG 780
GCCTCCTCAG CATAAAGGTG CTGGAGGGGG TCATCTCTAC CCTGCCTGCC TTAGGGAGGA 840
TGGTAGGGAC CAGTAAGGAT AAAGCATGGG AAAGTATTCC CAGAAACCAC AGAGGATTAC 900
CATTCTCTGA GGCCAGGCCT TGGGAAAGGA GGTCTCTGAT GAAAGCTGAG TGAGGACACA 960
CCCTTGCCTG CTGAACTCTG TGAGGGCAGG GCCCTGCGGG AAGACAGCAT TCCAGCCCCA 1020
GCCCTGCCTC CCTGCAGGAC CAGAATTCTG TCCTAGACAT GGCTGGGAGT CTCCGGAAAG 1080
GAAGGCACCC TCCCAGCAGG ACTATGTATG AGTCCAGGAG AAGTGTTGGG TCTGAGCCCA 1140
CTTCCTGAAA CAGGTATTAT ACTTCCTGTG CCACGACTTC CTGACCAGAG GGAGAACTCA 1200
AGCCTCCACA GGCAGGAAGA GCCCCGAGGG CAGGGCCCAG TATGGCCACA GCTGAGATGG 1260
CACGAGGGGC ACCCAGTGGA TGGTTCTGGG CTGGAGAGAA GCAGTGAGTT AGGGCCTCTG 1320
GGCACGGTGG ATTGAAGCAC TTCCTCTGGA GGCCTCAGCT GGGCAGGGGC AGGTCTTGGG 1380
CTCTAACCAC AGTGCCAGGA AAGAAAAGGG GAAGTGTCAG CTGCTACTCT GCTGAGAGGT 1440
GCTCCCCGAA GCTCCCCTCT GGAATCCCGA TTTTCAAGAA CACGGAAGGT CCCTGCCAAC 1500
CACCAGTCAC CATAACAGAT TGCTGGAGAG CAAGCTACAG CTCACAGTAA GAGCCAGAGG 1560
AATGATGAGG CAGGGAAACA GAGCCAGAGT CAGGCAGGAA GCAGGTGAGG AATAACTGTC 1620
TTAACATTGT TTTTTAAAAA AGAGATAGGC TGGGTGCAGT GGCTCATGCC AGTAATTCCA 1680
GCACTTTGGG AGGCCAACGC ACATGGATTG CTTGAGCTCA GGAGTTCCAG ACCGGCCTGG 1740
GCAACATGGT GAAACCCCAT CTCTACAAAA AATACAAAAA TTCGCCACGT GTGGTGACGT 1800
GCCTGTGGTC CCAGCTACTT GGGAGGCTGA GGTGGGAGAA TCACTTAACT CCAGGAGTTC 1860
GAGGCTGCAG TGAGCCAAGA TCATACTGCT GCACTACAGC CTGGGTGACA GAGTGAGACC 1920
CTGTCTCAAA TAAATAGTTA GATAGATAGA TAGATAGACA GACAGACAGA CAGACAGACA 1980
GACAGACAGA TAGATAGACA GATAGCTATA GAGAATAACA AGCAAGAGCC CAGGTCTGGG 2040
TGAGCCTCTC CTCTCATAGC ACAGGGCTTC ACCATCTACG ATACAGTCTA CGAAGCACTT 2100
ACCACCACTT CGTGGGGAGC AACAGGATTA TCACTCCCAT TTGGCCAGAG AAGCTGAGGC 2160
TGAGAGGGTG AAGTGACTTG CCCAGAAGTT CCACAGTTAG CCACAGGTGT GAAGAGAGGA 2220
AAGGAGTGGG GCTGGGCCCA AGTCTATATG CCTGACTGTC AGTCCTGAGC TTTCTGTGAG 2280
GCCCGGCAGC CAGCTGTGCC AGCCTGGATC AGACCAGAGT GTCAGCTGAT GAGAGTGGGC 2340
AATAGGGTTC ATTCTGTGCA TTAGGAACTT GTACAGAGAG ACCCTAGCTG TAAGGCTCGG 2400
AACAGGCCTC CTCTAGGCCA GGTGGTAACA CCATGCTGAG GGCAGCCAAG GATATCAACA 2460
CACACACACA CTTAAGAGTG GTGGGCAAGA ATGTTCCCAC AGGGCAATAG AGCTAGTGTC 2520
TAAAGACAGC CTCACTTGAA 2540