EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS100-00339 
Organism
Homo sapiens 
Tissue/cell
HT1080 
Coordinate
chr9:38007320-38010170 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs4878734chr938010085hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
INSM1MA0155.1chr9:38008209-38008221TGTCAGGGGTCA+6.18
RFX1MA0509.2chr9:38008279-38008295GGTCGCCATGGAAACC+6.14
RFX1MA0509.2chr9:38008279-38008295GGTCGCCATGGAAACC-6.16
RFX2MA0600.2chr9:38008279-38008295GGTCGCCATGGAAACC+6.47
RFX2MA0600.2chr9:38008279-38008295GGTCGCCATGGAAACC-6.57
RFX5MA0510.2chr9:38008279-38008295GGTCGCCATGGAAACC+6.15
RFX5MA0510.2chr9:38008279-38008295GGTCGCCATGGAAACC-6.25
Number of super-enhancer constituents: 31             
IDCoordinateTissue/cell
SE_00446chr9:38007447-38010016Adipose_Nuclei
SE_02310chr9:38007428-38010086Astrocytes
SE_03893chr9:38005034-38010007Brain_Anterior_Caudate
SE_04803chr9:37992427-38013214Brain_Cingulate_Gyrus
SE_05785chr9:37982493-38012896Brain_Hippocampus_Middle
SE_06784chr9:38005821-38008046Brain_Hippocampus_Middle_150
SE_06784chr9:38008147-38009676Brain_Hippocampus_Middle_150
SE_07767chr9:38007227-38010154Brain_Inferior_Temporal_Lobe
SE_26555chr9:38004284-38009915Esophagus
SE_27864chr9:38007504-38010171Fetal_Intestine
SE_28791chr9:38007411-38010540Fetal_Intestine_Large
SE_31580chr9:38007863-38009628Gastric
SE_33929chr9:38008349-38009123HCC1954
SE_34811chr9:38004680-38010190HeLa
SE_36884chr9:38007253-38009902HMEC
SE_38030chr9:38007224-38010273HUVEC
SE_40993chr9:38007705-38009501Left_Ventricle
SE_41666chr9:38007633-38009640LNCaP
SE_42283chr9:38004734-38009641Lung
SE_44329chr9:38007486-38009774NHDF-Ad
SE_44779chr9:38007207-38010197NHLF
SE_45758chr9:38007228-38010463Osteoblasts
SE_47196chr9:38008366-38010053Panc1
SE_51847chr9:38007784-38009405Skeletal_Muscle_Myoblast
SE_55662chr9:38006771-38012000u87
SE_57367chr9:38007912-38008398VACO_503
SE_57367chr9:38008499-38009382VACO_503
SE_63571chr9:38007784-38009601HSMM
SE_65279chr9:38007243-38009665Pancreatic_islets
SE_67542chr9:38006771-38012000u87
SE_69063chr9:38007826-38009440H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr93800776938009820
chr93801004838010110
Number: 1             
IDChromosomeStartEnd
GH09I038005chr93800513038010528
Enhancer Sequence
TACTGGGCCC AGAAGAGAAA TGAAGATGGG TGAGGACCAG TCCCTTCCTT CACGGAGCTC 60
TCGGCCCAGA GAGGGAAGGA AAAGAGGCAG AATCAGCTAT CCCTATGCAG TCCGCCGGCT 120
GCGGAGACAG AACTGGTCAG AACGCCCACC CAACTCCCAC CCTGACGCCA AGGCAGCCTC 180
CCTGCCCACC TAGCAAGTGG CTAAACTCAG ACTTTCCAGA TCTGGCATTC TTTGGAGGAG 240
GATAGGAGGT CCCTGGGCTC CTGAGGGGCA CCCAGGACTC TGTGGACCAG CCCAGGTCCC 300
AGGAGTGAAT TAATGCACTC ATTCATTCAA CCAGTGTTTA CTGACAACCT ACTTTGTACC 360
AGGTACTTCA GGTTCTAACA GGGAACAAAA CCTATATCTC TGCCCTTGTG AAGGCCACAT 420
CTCAGCAGTG AGACAGACAA CAAACAAGGG AAATGTAAAA AAAGTATGTA ATATGCTAAA 480
TAATGACAAG TGTTAAGGAA CAACATCAGA GAGGTGGGGG AGGGGTGGAA ATGTAAGATA 540
AGTGGCCAGA AGGCCTCCCT GAGGAGGTCA TTTTGAGTCA GGACCTCAAG CTTGGCTTTG 600
CTGGGATGCT GCCCTCTTTG TGCAGCACAC TTTGGTCCCA GAGGCTGTAC CACTCCTTCT 660
TCTGTGTTCT CCAAGACCAG ATTTCTCTCT CCAGTGTAAT TTTTCTTAGT TTGTTTTATA 720
CTACAGACAT CAAGTGTTCT CTGGGCCCCT GTCCACCTTC CCCATGTGAC AGGAGCACCT 780
GGAGGGCAAG GACCCTCAGC CCACAGCGGG GGTGCTATCA ATGACTGTCT GCTCTCCTTG 840
GCCTATTCCA GGCCTGCTGC AACTTTCCTG AAAACCTGAA CGTGCTCAGT GTCAGGGGTC 900
AAAGACAAGA GGGGAGCCGG GGTGAGAGAA TAGGAAGTGG CTCCTAGAGT GGGCCCGCTG 960
GTCGCCATGG AAACCCAGGC TTCCCACTTC TCTCCCCGCC CACAGCTCTG CGGGTGAGCA 1020
CCACTGGGCT GGGTGTGTGA GCCCTGCTGT TTCTTAAGAA TAGGAAAGTC ATCAGGTGAC 1080
TAATATGAAA TCTATTTACA CTTGATGATC TCCTTCCTGT CCGGTAGGTA AGTCATTCTG 1140
GCAAATGACA GACCAGCCAG GGAACTCTGC ACAGTCTACG ACCAAGCCTG CTACCTGCCA 1200
GGCAGGAGGA TTGACAACAG ATTTCACAAC ATTTCAAAAT AAGGCCCAGG AGCTCCAGGA 1260
TGGAAGTCAG GAGACTTGCC CTGTGGCTTG CTGCTGTGTA AACTTGGCTA GTGCACAACC 1320
CTCTCTGGGC CTCGGGCAGG AAGCCTATAT GGGGCCAGAA GCACTGCTCC TCAAGGACAG 1380
TTCCATCCTG CCATGATCCA GCTGGGGGAG AGCTGTGACC ACCAGGACAG GCTGAAGCCT 1440
GTGGTGTCTT GGTGGGGAGG GCAGGCCAGG GAGGAGCTTG AGGCCTGGAG AGGGTGAGAG 1500
GCAGCAGGAC AGAAGGAAGT GAGGGGGCTC AGGGTACAGG CTTTGGGGAG CAGAGCTGTG 1560
CAGGGAGGCA AGTGTGTGGA CATCCTGGGA GCAGAGTCCA CGGCACTACA GAGCTGGGGC 1620
TGGGAATGGC CTGGACTCAG GACCCAGACA GAAGGCCCTT TGCTTTCCCA GCTCAGGGGA 1680
ACAGTGCTGC CTGGAACCAG GGGTCAGGGC TGACGGCAAA TATGAGAGGA AGGCTGAAGT 1740
CTCAGGCAGG GTGGCCAGAG GCAGCTTCTC TGACACCCAA GCAAGACTCA CAGGCTCCTT 1800
TTTCTGAGAA GCATTTGCCG GTCTCCGGGA GAGTTCATTC CAGAATGAGA GAACAGGAGC 1860
CCTAGGAAGG GCCTCTAGAG CTGGCTGTCC AGAATGGTGT CCTGTCTGTC CTGAGAGCAG 1920
AGACAGCAGC ATGCATGCTT TTGGGAGGGG CTGAGGCTGA TGCCACATGG AGGTGGCTGG 1980
GGGTGGGGCA GGACCCTCAG GACTGTTAGA ACCAGGCCTG ACAAGGGCAG CTGGAGAAGC 2040
CCAGTGTGAC CGCAGAGGCG GGTAACCAAA GGATTTATGA AGTCACTCCA GACCCATGAC 2100
CTCTAAGAAT CCTCTTGACA CCCAGTGAAG GAGGCAGAAT CTGATTTTAG AGATGAGGGA 2160
ACTGAAGCCC AGAGAAGAGA AGCAACCTGC CCAAGGGCAG AGCCAGGGGC AGAGCCAAGG 2220
CTAGAACCTG TACTTCCTGC CTCCTTTCTC CTGAAACACA GAGGCCACAA TTGGAACATC 2280
GTCTTTAACA TGATAAACCC CATGATTCTC CCAGAGAGCA TGTTGCCACT AGAAGAGGCC 2340
ACACCAGAGG ATGAGAAAAT ACAAAAAAAA TCCCCTCTTG CCTTTAAAAT CAGTGACTGG 2400
CTTCATCTGG ACGGTGCCTA CTAGCACACA GTTAAAAAGG GCAGAAGGCC AGTTGTAAGC 2460
AAGGAAAACA GCCACGTCAA AGCAGGGGGG CTCTGTGTGA AATGACTTTA ATTTCCTCTT 2520
ATTAGGCTAT AAAGTTGATT TAATAATAAA AACATGCTAA GGACTTTTTA ATGTGTAATT 2580
GCTTACATAT TAAAAATTAT GTGAAAATGC TTTCAATTAA TGCTTAAAGA TTCATCCTGT 2640
GAGATGACAC TTTGAACAGT TTTATAAAGG ATGCCAGAGG AAGGGTTAGT AACATCTAAA 2700
AAGGCGGCCT AAGTAACTAA ATTTTCCAAT TATTCCTCAG ACTCTGGGGA ACACAGGACA 2760
GATGAGAGAG TGTTTTAGTT GTAAGCGAGG GCTCCAGAAG GTGCATCTTG GTTCTGTTTC 2820
TGCTGCTTAT TTAATCTGAG GCTCAGTATT 2850