EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS091-06288 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr10:104353820-104356890 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EBF1MA0154.3chr10:104356641-104356655TTTCCCTTGGGATT-6.25
KLF4MA0039.3chr10:104356384-104356395CCACACCCTCT+6.02
Nr2f6(var.2)MA0728.1chr10:104354695-104354710CGAACTCTTGACCTC-6.24
Pou2f3MA0627.1chr10:104354055-104354071TTGTATGTAAATTATA+6.07
ZfxMA0146.2chr10:104354720-104354734CCCGCCTCGGCCTC+6.01
Number of super-enhancer constituents: 23             
IDCoordinateTissue/cell
SE_00121chr10:104354819-104365558Adipose_Nuclei
SE_03928chr10:104355602-104356799Brain_Anterior_Caudate
SE_05850chr10:104351455-104354464Brain_Hippocampus_Middle
SE_05850chr10:104355359-104357883Brain_Hippocampus_Middle
SE_06794chr10:104353303-104354177Brain_Hippocampus_Middle_150
SE_06794chr10:104355019-104357193Brain_Hippocampus_Middle_150
SE_13930chr10:104354752-104355856CD34_Primary_RO01536
SE_13930chr10:104356228-104365014CD34_Primary_RO01536
SE_26660chr10:104356306-104357825Esophagus
SE_29332chr10:104355721-104357828Fetal_Intestine_Large
SE_29601chr10:104356201-104357859Fetal_Muscle
SE_31421chr10:104356316-104357096Gastric
SE_38034chr10:104355580-104361622HUVEC
SE_40696chr10:104355479-104358134Left_Ventricle
SE_42120chr10:104354666-104358341Lung
SE_48604chr10:104355618-104357942Right_Atrium
SE_50092chr10:104355613-104357967Sigmoid_Colon
SE_51270chr10:104356069-104357961Skeletal_Muscle
SE_52411chr10:104355607-104357807Small_Intestine
SE_53301chr10:104356190-104364847Spleen
SE_54642chr10:104354045-104358063Stomach_Smooth_Muscle
SE_65286chr10:104355437-104356030Pancreatic_islets
SE_65286chr10:104356220-104358092Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr10104354364104354544
chr10104355164104355404
chr10104356161104356563
Number: 3             
IDChromosomeStartEnd
GH10I102592chr10104352215104353957
GH10I102594chr10104354337104354501
GH10I102595chr10104354850104366005
Enhancer Sequence
AAGTATGTCT TGAGTGAGGA AAACCTTTCT AGCACCCTGT GCCTAGGCCT CTTCCAAATA 60
ACACTGGCTT TCATCCTGGG AAAACAGAGG ACCTTTATGT GTGAGTGAGT AGAAATATGG 120
CATCACTTGG AACTTGTCCC CTGAATTCTG CAGAGCACGT AGGGAGCAGA GGTTTCAGCC 180
CAGGAAAGCT AGTCCTCAGA CATATGTATT TTGGCATTTT AAAAGGATAT TTTTATTGTA 240
TGTAAATTAT ATATTGGCTT AAAAAATTAG ATTGCCAGCA ATAAAAGATA AGTGTAGTGG 300
ATATTGCTTG CTTGCCCAGT ATTCATTCTC CTGCCTCCCA GACTTTCTTT TAGGGAGCCA 360
CCACGGCCAC CACCGCCCTG TACCAGACAG TAGTGTAGGT GATACTGACT CCATGGCTCA 420
GCTGCAGGAG TGAGGGCTGA TTGGTCTAAT GGTCCTATCC CCATTTTCGC CACATTTTCT 480
ATCTTGGACA GTCAGATGCA GAGCTCCTAG CCTGGAAAGA TTGGCACCTT AGACACACAG 540
GCTGGCAGCT GCCCACTCCC TGTGGCCCAC CTGGACATTG TTTCAGTGTC ATCTTTGCTG 600
TTTTAGAAGC ATTCCTTTGT CATGCAGGTA AAGTTTGAAA GCCACAAGAA CGTAACTGCC 660
TTTTCTTTTT TTGAGACGGA GTTTCGCTCT TCTCACCCAG CCTGGAGTGC AGTGGCACAA 720
TCTCGGCTTA CTGCAGCCTC CGCCTCCCAG GGTCAAGCAG TTCTCCTGCC TCAGCCTCCC 780
GAGTAGCTGA GATTACAGGC GCCCACCACC ACGCCCAGAT AATTTTTTGT ATTTTTAGTA 840
GAGACAGGGT TTCACCATGT TGGCCAGGCT GGTCTCGAAC TCTTGACCTC AGATGATCCG 900
CCCGCCTCGG CCTCCCAAAG TGCTGGGATT ACAGGTTTGA GCTAGTGCGC CTGGCCCATA 960
ACTGCCTTTC TTATGGGCTT CTCTTGAAGC AGGAGCCACA GACAGCTAAT AATGTTACCT 1020
GCCTGGTGTC TGGCTCCTTC TACTCCCCTG ACCAAATGCA GGTCATTGCC ATCTCTAAAC 1080
CTGCCATGCT TCTGTAAAAT ATCTGGTAGG CCACAGGCAG TTGCCGGGAG TTCCATGTGT 1140
TAGAGCAAGA GAAAGGTGGC AGATGGACAT GTAGCCAGCA GCCCCTGAGT TCTTCACTGT 1200
AGACTTGTGA GTTCTTGGGC ATAAATCCTC TTCATTCACA GATGATGCTC CTCTGTTTTC 1260
CTAGTGCCTT TAACACTGAA CATTTCAAAC TGCTGCCAGG ATCCTCTGTT CTCTCTGCTT 1320
TAAACTTGGT TTCCTTGTAT CTTCTGCATA TGCAAGAACC AGGAACCAGG AAGGCTATCT 1380
TTCCCTAAGC CCTTGTTCTG TAGCCACACT GGGATCCAGC ATGGGGCACT GTGGGCCGTT 1440
GTTTGGCCCC TGTCATAAGT GCCAAGTACT AAGAAAGAAC CTGGTCCTTT GCACTAGTAG 1500
GGTAAACAGC TGTCCTTCCA TGCCAAGGGC TGTTCTTCCT AGTCTGCAGG ATCCCCTGAG 1560
AGCAGCCCAC AGGACCCGGA GCACCTAGTG GTCTTTGAAA GCAAGCCAGG GTCCCACAGG 1620
AACAAAGGAC AGCTTTCTTT CCTGGTGGCT CTGTGCACCA AGTGTGAACT CCTCTGTATT 1680
CACTGTGCCT TTCTGGGGCC TGCTTGCTAT CAGTCTCTTT AGAGCTGGCA TATATTCCTG 1740
TGATTCAAGC TCTACACTAA CCAGCTGTGT GCCCAAATAA GTCCCTCGCC TTCTGGGTCT 1800
TAACTTTTTC TTTTTACTTA TAAAGTAAAT AGCCCAGACA AGTTGAGCCA AGAATTGTCT 1860
GTCTGCAACT CTTTACCTAA GTGAGGGACC CCAGGGCAGC CAGTGCAGAG GAAAAAGCTC 1920
AGACTATCCC CTGAGCACAC CAGGGTATAC ATGCTCCCTG CCCAGAGTAC ACAGAGCGCT 1980
TCCCTGCTTA GCCTCTTCCT GCTCGGAACC CACAGCTTTG CCCAGGCCAG CATTAGCACT 2040
TGAAAGGAGG AGATGACTGA TGGGAAGGAG GCGTCTGGGG CAGAGCCACT TGCTGACTGG 2100
TCCCAGGAAA TAAGGACAGT ACCTGTACTT CTCCCACATG GGGCTTCTGG GCTGATCAGC 2160
AGGCCAGTGT GGTACCTGTG GAGCCGGGAA GCACAGATTA TTGTTGAGAT GCTCAGTCAC 2220
AAGCTTGATT TGGCCCACAT GGACATAGAG CCTTCCAGAT GACTTTTAAT TCAAGGTCCA 2280
GCATCAATGA ACTGTGTTTT ACCAGAAAAT CCAGGGATGT TTTGAGTACA ACTCTTCCTT 2340
GAAGCCATTT GGAGAGTGTT TGTACTCAGC AGTACCAAGG CCTGCACAAA GGCAGGGTCT 2400
CGATGGGGAG AGAAGGGTGT CTGCAGATAG TCACTGCACT CTAGGCCCCC ATTTCAGTCT 2460
AAGAAATGGG AAGGAATCTC CATCCAGAGT CCTTTGCTAA ACAAGGGAAC CAATGCATCT 2520
AGGGAAGTCC AGCCTTTGTT CTCCAGTGGC TCTTCCCTGT GTGACCACAC CCTCTAGCTG 2580
TTAGAAGGGG AAACTGCAGG TGTGGCCTGT TGCCTGTGGC AGGCTTCCAC CCTGTTTTCT 2640
ATAGCAGTGA CTGGGAGGTT CTGCCTGAAG ATCGGGAGGA GAGGAAGGAT CACACCTCTC 2700
CTCAGAGAAG TAGGCTCTCT CATGGCCACA TCAGCCCCAC CAGCCAGCGT GGCGGGGACA 2760
GGTTTGGGGC TCTGAAACAG GTAGAGGCCA TTGTGCTGGA AGGCTGATGG TAGAAGAGAT 2820
GTTTCCCTTG GGATTTGCAT TCCTCCTGGC TTCCCCTAAT CCCTGGTTCC CCTGGAGGAG 2880
TCCAGGAGCT GGCAGAGACC ATCATGCATT GGTAACCAGG GCAGAACAAG GTCAGAGATC 2940
CTGCTCTCCA GCATTTGTCC CATGCTCAGC ACCACAAGGG CTCAGTAAAT ACTGTAAGAG 3000
CAGTGGCTGA AAGGGTGGTC ACCTTGGGTC ACCAGTTCTC TGAAAGAACT CTGGCTCTTT 3060
GGTTCTTTTC 3070