EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS110-05046 
Organism
Homo sapiens 
Tissue/cell
KATO3 
Coordinate
chr9:127027880-127031100 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs12379417chr9127029736hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GabpaMA0062.2chr9:127028731-127028742CCGGAAGTGAC+6.14
MYCNMA0104.4chr9:127030909-127030921GGCCACGTGGTG+6.07
MYCNMA0104.4chr9:127030909-127030921GGCCACGTGGTG-6.07
Nkx3-2MA0122.3chr9:127030559-127030572ATTAAGTGGTTTA-6.92
RUNX1MA0002.2chr9:127029896-127029907TTCTGTGGTTT+6.32
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_01861chr9:127028027-127030811Aorta
SE_02294chr9:127028292-127030548Astrocytes
SE_03002chr9:127027842-127028520Bladder
SE_04593chr9:127028891-127030342Brain_Anterior_Caudate
SE_06625chr9:127028933-127030320Brain_Hippocampus_Middle
SE_09789chr9:127025946-127031287CD14
SE_23712chr9:127027894-127031158Colon_Crypt_1
SE_24006chr9:127027853-127028277Colon_Crypt_2
SE_24006chr9:127028279-127028609Colon_Crypt_2
SE_24006chr9:127028617-127030420Colon_Crypt_2
SE_26169chr9:127028464-127031167Duodenum_Smooth_Muscle
SE_27460chr9:127028546-127029502Esophagus
SE_27460chr9:127029577-127030298Esophagus
SE_29975chr9:127028907-127030325Fetal_Muscle
SE_31765chr9:127027836-127031189Gastric
SE_36996chr9:127027502-127031245HSMMtube
SE_38009chr9:127027450-127031685HUVEC
SE_38868chr9:127028106-127031763IMR90
SE_42506chr9:127027674-127031138Lung
SE_44293chr9:127028727-127031058NHDF-Ad
SE_44809chr9:127028276-127028828NHLF
SE_44809chr9:127029011-127029548NHLF
SE_45648chr9:127018281-127031420Osteoblasts
SE_47283chr9:127027822-127030793Panc1
SE_47557chr9:127029471-127030049Pancreas
SE_50283chr9:127027697-127031101Sigmoid_Colon
SE_51779chr9:127028340-127030620Skeletal_Muscle_Myoblast
SE_52726chr9:127027715-127030348Small_Intestine
SE_54297chr9:127028449-127030673Spleen
SE_59258chr9:127016097-127031007Ly3
SE_60141chr9:127018983-127030974Ly4
SE_60448chr9:127019058-127056389DHL6
SE_63558chr9:127028209-127030812HSMM
SE_65907chr9:127028092-127030478Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr9127028281127028331
chr9127028725127030267
Enhancer Sequence
AGACATCATG ACCAGCCTCA GGTCCCACAT GCAGCCTGCT GCTCTGTAGC CTAAATCAGA 60
TCACTGTCCC AGCTTTCAGG TCAAGGCTCT GGTTGTGACA CCTGGGCCTG GACTGCGGGT 120
GAAAAGTTTT GATGCAAAAA CACAGACCGT CCATTGTCCT ATGGGCTAAG TGGACTCCCT 180
TCTGCTAACC AGAGATGCTT GTGCTGGCTG GTGTGTGGCA CGTTATCTCA TTCTTTCATG 240
ACGTATGTCC GGATGGAAGT CCTGGGTCAG GCATTGTGCT GGGAGCCCAC ACGAAGACCC 300
TCTAATGGCC CCACCCATTG GCCTCTCACC ACCTGGTGGG GACAGAGGCT GTCACAACCC 360
CTTCTTAGGT GCTCTTGATC AATTTGCAGG TGGCATTTTT TGGGATGTAG TCTCTGGGGA 420
AGTAGGAGAG CTTCCGGCAG TGAGGGGTGT TTGAACCCAC CTGGAGGGAG ACGTGGGGTT 480
TGCCAGAGGG CTGAGAGGGC TGGGGTGAAG GGCAGGTAGA CCCCAAGGTG GAGAGGCAGG 540
TGGGGCCGGT GGGTGAGAGG TGGGGCTGTG GAACTTCCTC CTGCTTCTTT GGCCTTTGCT 600
CCTGTCGGTA GATGGCCTTA CCAGGCACTT ACTGTGGGCC ATGTTCTAAT CTAACCCTTA 660
ACCTGAGGGA ACTCACTTCA TCCTCCCAGT GATGCCGTGA TGTGGGTATC GTTCTGCCCA 720
TTTTATAGAT GAGGAAACAG AGACCCAGAG AGTCCAGGAT CTGTGGTGCT TGACGAGCAT 780
CAGCCTGAGT GCTGTGAGGA CACCCACAGC ATGGGGGTCT GAGCTGAAAA TTGGAGGACA 840
GAGGCTGCCC TCCGGAAGTG ACCAGGATGT GCCCTCAGGA AGTGACCAGC TGCCCAGCTC 900
AGGACCTGTG TGAGGGCCCC CAGGCAGCTG GAAGGAACAG TGTGCACCCA GGTACCATGC 960
CAGGGCCCCT GAGCATCCGT CTTGTCATCG CATAGTTGTA ACCTGCCTCA CAGACTGAAC 1020
ATGCACTCTA GAAGGGGATG GGACTTGGTC TGTGGACCAC AACAGTGTTC TCCATGGCCA 1080
GCATTGTGCC TGACACATAG GAGGAGCTCA ATTAATATTT GTTGAGTGAA TGGGAAGTTT 1140
TAAGTAGGCA CGCGGCCGGA TCCTTGGAGA ATGTTTATAT GGAGTGAACG AATCTGTTAG 1200
CAAACGTTCC TCACTCCCCT CAGTGGGCTG TGCAGGGCTG TATTGAGCTG AGCTGGCCCT 1260
TCCCTGGGAG AAGAGGTTTC TTAGAGAAAT GCTCATCCTC GAATTATTCC AATGAGGAGG 1320
AACCTAAGCC CAGAAGGGCT CTACCTCCCA GAGTTACAGG CTCTCCTTCC TATGCCCCTT 1380
CCCTGCCGAG GCAGCTCCCA CATGTCTGCA TAGGAGGGCT TTGGGTTGGA ATGGGTCAGT 1440
GCTGTGTCTT AAAGCTGCAT TTTCTACCAA GCACACACTT TGTTTAGAGG GCATATCTTT 1500
TGGGGTTGCT TTGAGGAAAG GCTAACCAAG CCACCTCTGA GCACAGACAT GACTTTTTGG 1560
CAAATGAGCA GGACCCCAGA TTACACCCCA TCTTAGAAAG TAGGAAACCC AGCATTGAAA 1620
GAGGAAAGAT TCTGCAGCTG ATGTGGCCTT GGCGGGCCAC CAGCGTGGGT GCCCAGATGG 1680
CAGGATCACT GGGCACCACA TGGCACACAG AAGAGAGCAA AGGAGAGGGA GTCCGCCCCT 1740
GGGCTTGGCA GGTCCGGTCG AGTCCGCCTG GATTCAGTTA CAACAGGACC TCGAGTGGGC 1800
ACGGCGTGCC GGACTGAGTC AGTGTGTGTA CATTTCCTTT GTTCGTCTCC TCCGGGAATG 1860
TAGTGGCCTT TTGTGTGTGT TTTAAATGCC AGCCTCCTTA CCTAACCCAA GAGGAAATGA 1920
GGACTGGGTT TTTGTCTGTG CAGACGCTGG GACAAGTGTG GGAGCCGCCT GCTCTTGGAG 1980
CCAGCCTAGT GGTGACAGCG TGGCATTTGG AAAACATTCT GTGGTTTTCT CCAAGGGGTG 2040
ATGGGCACAC CAGGTGCTGG GCCGCCCCTG AGCTGGCCAC TGGGACCCTG AAATGAGGAA 2100
GCCCTGTGAC CAGGTTTCAT GATGCCATTC AGCAAGGGAC GGCTGAGCAC CACATGCCTT 2160
CTTGGCCCCT GGGGAAACAC ACAGGAATCA GATGAGGTCC CTGCCCCGTC TTCCTGGGGA 2220
AACATGCAGA GAAAATACTT GTACTCTGAG CTAACACCTT TCACTCGCAC AGACCTTTAT 2280
GGTGTTCTGT GTCTTCAGAC ATTGATCACC TGTAGGTGAG ACACATCATG GCCCCACTTT 2340
CCAAACTCCC AAACGGGCTG TGATCTGTAG AAGTATTTAG TGCCATTCAG GGACAGGAGA 2400
GATGGTTTGG AAGATGCTGT CTGCTGTGCG AAGTCTCTGG ATGCTCAAAT GGCTTATGGG 2460
GTGGCATCTT TGAAATTACC CAGTCCTGAA AATTTCAGGA CATATGGTCA CTGTGATGTG 2520
CTAATGTTAG CAATTGAGAT ATTTAATGAC CCAGAAAAAC CCCTTTTCCT ACCCAGTGCA 2580
GGTTACTGGA GAGCCTTTAT TTCTCAGGAG GAGGGTCTTA CACAGTGTAA TTTGGACCAG 2640
CAGATAGGGA GTCATTATCC CTCATTCATT TATTAGCTAA TTAAGTGGTT TATCTGGTCA 2700
CACATTTACT CCTTCAATTG CCATTCATCC AGCACTGTTT GCTGATGTAC CTGGCCTGGT 2760
GCTGGGTACT GGGGGTGGAA TGAAACAGAA CAAATATGAC TGAGTCCCTA CTGTGTGCCA 2820
GCCCATAGGG TGTGCTGTGT GCCACAGGTG AATGCATTCA CTTCCCAGTG GACATTTAAC 2880
AACCACCTAC TGTGTGCAGA CTCATGGAGA TGCAGAAATG CAAATGGCAC AGTCCGTAGT 2940
GGTTTGGACA CTTGTGGTGT TTTGATGGGG TCTTTAGTCC TGGCTCTCTC TCTGCTTGCT 3000
GTGATATACC CAGTCAGCCA CTGTTCACAG GCCACGTGGT GACGTCCCCA GAATGAACCA 3060
GAAACAATCC AGATGCCCCA GGAACCGACG TGAGAACAAG GCATCCCCTT CACACGTTGT 3120
GTCTCAGTTC AGCGTCTTGC CACCACCCAG CATTTTGAGA CAGAATGTGA GATCGCGTGG 3180
TTGGCTAAAT ACATAAATAT TTTATGTCTC GATATTCTGA 3220