EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-36724 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr22:30697110-30699800 
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
CCGCACAGGC TGGAGGGACC CAGCCCCGTG TACTTTCTAC ATCACCAGTG GGCTCCTCCT 60
GGGCTTGGGA CCAGAATGAG GCTCTGAAGG CAGTTGCCCT GACCCGTCAA GGTGGGCAAG 120
GACAAAGGCA GAGGCATCAC TCCTGTGAAA TGCTGTGGTG GGGGAGGGGT GAGATGGCCA 180
ATGATACTCC CTCAACCCCT GCACTAAGCA GCCTGACCTG GGATAAAGGG GATGGGCGCT 240
CGGGGCATGA GAAGAACATC TGGATGTGGG TTTGAATCTA GCGCTGACCT TAAGCCAACC 300
ACTTCTCAAC TGTAAGATCT GAATAATACC TACTACTGTG CAGAGTTGTC AAAGGAGTCC 360
ATTAGAGAGG GAAAATGTGC TTAGTGTGGG GCCTGACACA GTCTGTGTTC AGTAAGCAAT 420
GGCTTCCTCT CTGCCCCTCC ATCCCAGGAG GATGCTTGAC ACAGAAGCCC AGGACCTCAG 480
CTCACACCTA ACTTCCCCTC ACCTAGAAAC CCCCTTCAAC AGTCCTGCTG GAAGCTCTCA 540
GAGGAGGGAG TACAGAAGCC CTGGCCTTCC TGGGGACCAG TGCAAACAAG AGAAAACTTT 600
CCAAGGGTCA GAGAGAGTCA AGAACCAGGA AGGAGCCAGG CAAACAGGCT GAGGGTGGTG 660
GGGGAAGAGT AGCAGTGGCT GGTCACAGGT GCCAAGTGAG AGCTTCTGGG ACTGCCTAGA 720
AAGGAGGCAG AGGAAGGGGG CTGAAGGGAA CTGCACTAGA CGCAAGGAAG AGTTTCCTGC 780
GGCTATGGGA CAAGGGTCTC CTTAAGGAAG CCAACTTGGG CAGGCTTTGG CAAAGGGATG 840
TGCTTTAGCC CAAAGCCACA GGCCCTTCAG GCTCTCCCAC AGAGCTAAGC TCAGCAAGAG 900
GCAGCCCCAC ATCATCACAG CCCCCATCAT ATTTGGCCTT CTCCAGGAGA GCCCTGGAAC 960
ACTTCGCGGG CAGCAAAGAG CTGGGAGTAC AGCCAGCCTT TCCCACTCTG GCCTCCTCAG 1020
CATAAAGGTG CTGGAGGGGG TCATCTCTAC CCTGCCTGCC TTAGGGAGGA TGGTAGGGAC 1080
CAGTAAGGAT AAAGCATGGG AAAGTATTCC CAGAAACCAC AGAGGATTAC CATTCTCTGA 1140
GGCCAGGCCT TGGGAAAGGA GGTCTCTGAT GAAAGCTGAG TGAGGACACA CCCTTGCCTG 1200
CTGAACTCTG TGAGGGCAGG GCCCTGCGGG AAGACAGCAT TCCAGCCCCA GCCCTGCCTC 1260
CCTGCAGGAC CAGAATTCTG TCCTAGACAT GGCTGGGAGT CTCCGGAAAG GAAGGCACCC 1320
TCCCAGCAGG ACTATGTATG AGTCCAGGAG AAGTGTTGGG TCTGAGCCCA CTTCCTGAAA 1380
CAGGTATTAT ACTTCCTGTG CCACGACTTC CTGACCAGAG GGAGAACTCA AGCCTCCACA 1440
GGCAGGAAGA GCCCCGAGGG CAGGGCCCAG TATGGCCACA GCTGAGATGG CACGAGGGGC 1500
ACCCAGTGGA TGGTTCTGGG CTGGAGAGAA GCAGTGAGTT AGGGCCTCTG GGCACGGTGG 1560
ATTGAAGCAC TTCCTCTGGA GGCCTCAGCT GGGCAGGGGC AGGTCTTGGG CTCTAACCAC 1620
AGTGCCAGGA AAGAAAAGGG GAAGTGTCAG CTGCTACTCT GCTGAGAGGT GCTCCCCGAA 1680
GCTCCCCTCT GGAATCCCGA TTTTCAAGAA CACGGAAGGT CCCTGCCAAC CACCAGTCAC 1740
CATAACAGAT TGCTGGAGAG CAAGCTACAG CTCACAGTAA GAGCCAGAGG AATGATGAGG 1800
CAGGGAAACA GAGCCAGAGT CAGGCAGGAA GCAGGTGAGG AATAACTGTC TTAACATTGT 1860
TTTTTAAAAA AGAGATAGGC TGGGTGCAGT GGCTCATGCC AGTAATTCCA GCACTTTGGG 1920
AGGCCAACGC ACATGGATTG CTTGAGCTCA GGAGTTCCAG ACCGGCCTGG GCAACATGGT 1980
GAAACCCCAT CTCTACAAAA AATACAAAAA TTCGCCACGT GTGGTGACGT GCCTGTGGTC 2040
CCAGCTACTT GGGAGGCTGA GGTGGGAGAA TCACTTAACT CCAGGAGTTC GAGGCTGCAG 2100
TGAGCCAAGA TCATACTGCT GCACTACAGC CTGGGTGACA GAGTGAGACC CTGTCTCAAA 2160
TAAATAGTTA GATAGATAGA TAGATAGACA GACAGACAGA CAGACAGACA GACAGACAGA 2220
TAGATAGACA GATAGCTATA GAGAATAACA AGCAAGAGCC CAGGTCTGGG TGAGCCTCTC 2280
CTCTCATAGC ACAGGGCTTC ACCATCTACG ATACAGTCTA CGAAGCACTT ACCACCACTT 2340
CGTGGGGAGC AACAGGATTA TCACTCCCAT TTGGCCAGAG AAGCTGAGGC TGAGAGGGTG 2400
AAGTGACTTG CCCAGAAGTT CCACAGTTAG CCACAGGTGT GAAGAGAGGA AAGGAGTGGG 2460
GCTGGGCCCA AGTCTATATG CCTGACTGTC AGTCCTGAGC TTTCTGTGAG GCCCGGCAGC 2520
CAGCTGTGCC AGCCTGGATC AGACCAGAGT GTCAGCTGAT GAGAGTGGGC AATAGGGTTC 2580
ATTCTGTGCA TTAGGAACTT GTACAGAGAG ACCCTAGCTG TAAGGCTCGG AACAGGCCTC 2640
CTCTAGGCCA GGTGGTAACA CCATGCTGAG GGCAGCCAAG GATATCAACA 2690