EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-58620 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr9:127028460-127031000 
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: 31             
IDCoordinateTissue/cell
SE_01861chr9:127028027-127030811Aorta
SE_02294chr9:127028292-127030548Astrocytes
SE_04593chr9:127028891-127030342Brain_Anterior_Caudate
SE_06625chr9:127028933-127030320Brain_Hippocampus_Middle
SE_09789chr9:127025946-127031287CD14
SE_23712chr9:127027894-127031158Colon_Crypt_1
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: 1             
ChromosomeStartEnd
chr9127028725127030267
Enhancer Sequence
CTGCTTCTTT GGCCTTTGCT CCTGTCGGTA GATGGCCTTA CCAGGCACTT ACTGTGGGCC 60
ATGTTCTAAT CTAACCCTTA ACCTGAGGGA ACTCACTTCA TCCTCCCAGT GATGCCGTGA 120
TGTGGGTATC GTTCTGCCCA TTTTATAGAT GAGGAAACAG AGACCCAGAG AGTCCAGGAT 180
CTGTGGTGCT TGACGAGCAT CAGCCTGAGT GCTGTGAGGA CACCCACAGC ATGGGGGTCT 240
GAGCTGAAAA TTGGAGGACA GAGGCTGCCC TCCGGAAGTG ACCAGGATGT GCCCTCAGGA 300
AGTGACCAGC TGCCCAGCTC AGGACCTGTG TGAGGGCCCC CAGGCAGCTG GAAGGAACAG 360
TGTGCACCCA GGTACCATGC CAGGGCCCCT GAGCATCCGT CTTGTCATCG CATAGTTGTA 420
ACCTGCCTCA CAGACTGAAC ATGCACTCTA GAAGGGGATG GGACTTGGTC TGTGGACCAC 480
AACAGTGTTC TCCATGGCCA GCATTGTGCC TGACACATAG GAGGAGCTCA ATTAATATTT 540
GTTGAGTGAA TGGGAAGTTT TAAGTAGGCA CGCGGCCGGA TCCTTGGAGA ATGTTTATAT 600
GGAGTGAACG AATCTGTTAG CAAACGTTCC TCACTCCCCT CAGTGGGCTG TGCAGGGCTG 660
TATTGAGCTG AGCTGGCCCT TCCCTGGGAG AAGAGGTTTC TTAGAGAAAT GCTCATCCTC 720
GAATTATTCC AATGAGGAGG AACCTAAGCC CAGAAGGGCT CTACCTCCCA GAGTTACAGG 780
CTCTCCTTCC TATGCCCCTT CCCTGCCGAG GCAGCTCCCA CATGTCTGCA TAGGAGGGCT 840
TTGGGTTGGA ATGGGTCAGT GCTGTGTCTT AAAGCTGCAT TTTCTACCAA GCACACACTT 900
TGTTTAGAGG GCATATCTTT TGGGGTTGCT TTGAGGAAAG GCTAACCAAG CCACCTCTGA 960
GCACAGACAT GACTTTTTGG CAAATGAGCA GGACCCCAGA TTACACCCCA TCTTAGAAAG 1020
TAGGAAACCC AGCATTGAAA GAGGAAAGAT TCTGCAGCTG ATGTGGCCTT GGCGGGCCAC 1080
CAGCGTGGGT GCCCAGATGG CAGGATCACT GGGCACCACA TGGCACACAG AAGAGAGCAA 1140
AGGAGAGGGA GTCCGCCCCT GGGCTTGGCA GGTCCGGTCG AGTCCGCCTG GATTCAGTTA 1200
CAACAGGACC TCGAGTGGGC ACGGCGTGCC GGACTGAGTC AGTGTGTGTA CATTTCCTTT 1260
GTTCGTCTCC TCCGGGAATG TAGTGGCCTT TTGTGTGTGT TTTAAATGCC AGCCTCCTTA 1320
CCTAACCCAA GAGGAAATGA GGACTGGGTT TTTGTCTGTG CAGACGCTGG GACAAGTGTG 1380
GGAGCCGCCT GCTCTTGGAG CCAGCCTAGT GGTGACAGCG TGGCATTTGG AAAACATTCT 1440
GTGGTTTTCT CCAAGGGGTG ATGGGCACAC CAGGTGCTGG GCCGCCCCTG AGCTGGCCAC 1500
TGGGACCCTG AAATGAGGAA GCCCTGTGAC CAGGTTTCAT GATGCCATTC AGCAAGGGAC 1560
GGCTGAGCAC CACATGCCTT CTTGGCCCCT GGGGAAACAC ACAGGAATCA GATGAGGTCC 1620
CTGCCCCGTC TTCCTGGGGA AACATGCAGA GAAAATACTT GTACTCTGAG CTAACACCTT 1680
TCACTCGCAC AGACCTTTAT GGTGTTCTGT GTCTTCAGAC ATTGATCACC TGTAGGTGAG 1740
ACACATCATG GCCCCACTTT CCAAACTCCC AAACGGGCTG TGATCTGTAG AAGTATTTAG 1800
TGCCATTCAG GGACAGGAGA GATGGTTTGG AAGATGCTGT CTGCTGTGCG AAGTCTCTGG 1860
ATGCTCAAAT GGCTTATGGG GTGGCATCTT TGAAATTACC CAGTCCTGAA AATTTCAGGA 1920
CATATGGTCA CTGTGATGTG CTAATGTTAG CAATTGAGAT ATTTAATGAC CCAGAAAAAC 1980
CCCTTTTCCT ACCCAGTGCA GGTTACTGGA GAGCCTTTAT TTCTCAGGAG GAGGGTCTTA 2040
CACAGTGTAA TTTGGACCAG CAGATAGGGA GTCATTATCC CTCATTCATT TATTAGCTAA 2100
TTAAGTGGTT TATCTGGTCA CACATTTACT CCTTCAATTG CCATTCATCC AGCACTGTTT 2160
GCTGATGTAC CTGGCCTGGT GCTGGGTACT GGGGGTGGAA TGAAACAGAA CAAATATGAC 2220
TGAGTCCCTA CTGTGTGCCA GCCCATAGGG TGTGCTGTGT GCCACAGGTG AATGCATTCA 2280
CTTCCCAGTG GACATTTAAC AACCACCTAC TGTGTGCAGA CTCATGGAGA TGCAGAAATG 2340
CAAATGGCAC AGTCCGTAGT GGTTTGGACA CTTGTGGTGT TTTGATGGGG TCTTTAGTCC 2400
TGGCTCTCTC TCTGCTTGCT GTGATATACC CAGTCAGCCA CTGTTCACAG GCCACGTGGT 2460
GACGTCCCCA GAATGAACCA GAAACAATCC AGATGCCCCA GGAACCGACG TGAGAACAAG 2520
GCATCCCCTT CACACGTTGT 2540