EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS116-05140 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr10:105424700-105428360 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs3781339chr10105428152hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr10:105426075-105426094TGCTGCCCCCTGCTGGAAT-6.54
STAT1MA0137.3chr10:105425137-105425148TTTCCTGGAAA-6.62
Stat4MA0518.1chr10:105425134-105425148CACTTTCCTGGAAA-6.36
Tcf12MA0521.1chr10:105428252-105428263AACAGCTGCTG+6.32
ZNF263MA0528.1chr10:105426636-105426657GGAGAAGGGTGGGGAAGGGAG+6.63
Number of super-enhancer constituents: 31             
IDCoordinateTissue/cell
SE_01123chr10:105427529-105429036Adrenal_Gland
SE_03245chr10:105424634-105425152Brain_Angular_Gyrus
SE_04829chr10:105422511-105429995Brain_Cingulate_Gyrus
SE_05806chr10:105422432-105430177Brain_Hippocampus_Middle
SE_06868chr10:105422459-105426110Brain_Hippocampus_Middle_150
SE_06868chr10:105427804-105429536Brain_Hippocampus_Middle_150
SE_07764chr10:105422452-105430753Brain_Inferior_Temporal_Lobe
SE_24302chr10:105427603-105428043Colon_Crypt_2
SE_27093chr10:105425077-105425825Esophagus
SE_27093chr10:105426800-105427346Esophagus
SE_27093chr10:105427350-105429189Esophagus
SE_28404chr10:105426356-105429142Fetal_Intestine
SE_29224chr10:105426080-105428942Fetal_Intestine_Large
SE_29876chr10:105424688-105429281Fetal_Muscle
SE_32187chr10:105426513-105429215Gastric
SE_37600chr10:105427474-105429617HSMMtube
SE_41304chr10:105424609-105426037Left_Ventricle
SE_41304chr10:105426389-105429198Left_Ventricle
SE_42617chr10:105426380-105429677Lung
SE_44236chr10:105427611-105429550NHDF-Ad
SE_44930chr10:105426679-105429496NHLF
SE_45960chr10:105425744-105429515Osteoblasts
SE_46694chr10:105425244-105425640Ovary
SE_46694chr10:105426546-105427464Ovary
SE_46694chr10:105427582-105429072Ovary
SE_49112chr10:105425984-105429683Right_Atrium
SE_50307chr10:105426286-105429281Sigmoid_Colon
SE_52745chr10:105426640-105429718Small_Intestine
SE_65658chr10:105424959-105425957Pancreatic_islets
SE_65658chr10:105426429-105429179Pancreatic_islets
SE_69111chr10:105426562-105429087H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr10105426889105427795
Number: 1             
IDChromosomeStartEnd
GH10I103665chr10105424821105429605
Enhancer Sequence
GATTATAGGC ATAAGCCACC ACGCCTGGCC TAGAGTATGG GTTTCTAGTT GACTCTTGCC 60
ACCTCTACTG ACCAGACCAC AGTGCCTGTT AGGTGGCAGG CACTCAATAA GTGTGAAATG 120
AACCAGTGAA ACGCGTGAAC TGGCAGAAAG ATGAACAGAG GGACTCATTG GTTTGTGGTG 180
TCAATATGAA TACCTTGACT CTGATATGGG AATATGGGAA AATGAGCCAA ACTCGAAGGG 240
AGAAAGGGGA GATGGGGAAA CTGAGGTAAG GAGGAGAAAG AAGCCCCAGC TTTGTGGCCA 300
GAAGATGCCT GGAGGACGAG CAGGAGGTGC TGGGGAGTGG ACAGACATCA GCTCATTTTA 360
ATCCAAGCCA AGAAAATCTG AGGCAGGGTT TCAAAGCAGA GTTAAATCCA CACCCCCACA 420
CCCCTTCCCC CCACCACTTT CCTGGAAAAT TGGCCTGACC TTCCTGAAGG CTGACTCTCT 480
GGGACACAGG TAGAAAAGTT AAGGAAATAT TCTCTAGGCA TTGGAAAGCA CAGACAGGCT 540
ATGGCCTCTC TCAGGAGCTG CTCCAAAGGC TGTGGGATGG ACACACGGAC ACTCTGTCCT 600
TCTGGCTGCC CTTCCCTCCC GTTGCACAGG CAGGCTCCCA GCTCTTCCCT CTGGCAGCTG 660
CCTCTTAGGG TGTTCCCTGG CCAGGGCAGC CGGGCGGGCG GGAGCTGCGA GCAGGTATCC 720
AGATGAGAAA CCACTTGCAG GCCAGGCAGG CAGTGGGCGG TGATGTCATC CCACAGAGGC 780
CACTCTGGAT CCCCTCTCAG CCAAGGCCTG CAGAACTAGG GGCTGGAGGA GTCTGCCTGA 840
GTGGGGAGGG GGCAGTGGAG GGAGCCTGGT GTCTTTAGAT GAGGAGTGCT TGGCAGGAGC 900
ATGGAGAAGG GGTGTACCTC TTCTAGACAG CAGAGCCTCT CCTGGGTTGG AAGGGGCCTT 960
TGCATGAGTC TGATCCAGAG ATGGACCCTT GTGCTTTATT ACAGAGCCCC TGGCTGGACC 1020
TGCTGGGGTC CCAGGGGTCC CCTGGACCCC TGCCCCACCC TTGCCTCACA TCTGCATTCC 1080
TTCAACTACC ACCTGGATGG AACCCTGGCT GCCAACTTAA ACTTCTCAAC TGGGCTTTTG 1140
CCAAGTCAGT CCCATGCTCC AACGCCTTCC ACGGCTCCCT CTTGCCTATA AAGGACAAAT 1200
TCAAGCCCAG TCTTTCTTGC CAATCTGAGC TCCCCAAGTT CCTTGATCCC CGTCCCCCAC 1260
ACCACCATTC AATACATCAT TCATGATTCA ACACATGTAT CGAGCACCCA CTAGGCGCCA 1320
ACACCCAACA CCACTGCTCC ATGCAGCTTC TTACTTTCCA AGTCTGTGCT CTAGCTGCTG 1380
CCCCCTGCTG GAATGCTTTC CCTTCTCTCT ACCAATCCCA GTTTCCCAAT TCTCCCCAAG 1440
CATCTCTGTC CTCCAGGAGG CTCCTGATCA CTCTTGTTCC CTCTTTTCTG TTCCCTCCTG 1500
GACTTTATGT TGGGCATTGC TCCCCAACCA AAGTATGTGC CTTGGACAAG AGTCTCTCGA 1560
CACTCCAGGA CTGGTGCCTC AGGACATGAC ATGGGACATA GTAATTACCT GAAATTCATG 1620
ATGGAAATGC TTAGAATTAG AGTCCAAAGG TCTGAGGTCC AGTCCTGCTT TGCCCTTACT 1680
AGCTCTGAGA TCCTGGGGAG GACACGTAAC CTCTCTTGAG CTTTAGTGTC ATCTGGAAAC 1740
AGGAACAATA GCAGTTCCTA CCTCATGGGA ATTGTTCTGA GCACGGAATG AAGTGACGGG 1800
GCTTCAAGTC CTATGGAAAT CATAGATGGT CATTTTAAAG CAAGTGGAGG GAATGGGAGA 1860
TCTGAGGAGC AGCAAAGCTG TTGGTTCCTT CGTGGGCTCA CCAGCAGGCA GCTCGGTGCC 1920
AGGGCTGCAG GTGCCAGGAG AAGGGTGGGG AAGGGAGGCC GGGGGCTGTG TCCCTGCAAC 1980
ATGCCCCTCC CAGACCCTAC CTTCAGCAGG TAACGGGTAC TTGCCAGCTG GATTGAGAGG 2040
CAGCTCAGAG CCCCCTGGGC CTACTCTGGG GGGATGCCAG GCTAAGCAAC CTGAGGCCCC 2100
TGATCTATAA GGATCTCCAA CATCAGCCCT TACCTCTGAG TTTCCTGTCT CATATCTCAA 2160
AGAACCCTCC AACCCTCCAG ATGGAGAAAC CAAGGCCCAG AGAGACTCTG GCCCTGGACT 2220
CGCAGTCTGG CTGGGTTTTC CCCCAGCCCA CACTGCCTCC CCTGGGCCTC TCACTCCAAA 2280
CAGCTGGGAT CATCTTGAGA CGTGGTTAAG TGTCCTCCCC AGGGTCACAG AGCTAGTAAG 2340
GCCCTGTGCT GGCCTCCACC CCAGGCTCCC CACGACTCCC CAACCCTGGG CATCCTACAA 2400
AAGTCCCTCT AGCCCCTTAT AACTGGTTCC TCCCAGGCTG GACTGGGACT GCTGGCCCCT 2460
CCGCTATACG TTTGGTGAAT AAAATGTATT GCTGTGGGCC AAGTGGGCTC TGGCTCACTG 2520
GCGTGTGGAG AGGGGAAAAA GGGACAGGAG CCCAGTGATT AGCTCAGGCC CAGGCCCTCG 2580
TCACAGGAAA CTCCAGAAGG AGATTGCAAC GCCCTCCGAC CCACTGCCTT CTCTTCTCCT 2640
CTGGACTCCT CCCAACACGT TTACCTCCCA TTCCCCGCCC ACAGCTGCAG CAGTAGGGGC 2700
TGGGCTTTGG GCTCTAAACA CTGGGGCTGG CCCAGCCCCA CCACCCCACT CAGCTCCCAC 2760
CCTTCTGCTT TGTCCCCTAT TCCCCCAGCC TGAACCTCTG CTCTCAGGTT TGGGGCTAGA 2820
GGGTCAGGGT GTGTAACAGC CTCAAAAATG GAGGGGTCCC ATAGAAGACC CTTCTGGAAA 2880
TTCCATCCCT CCTCCGACCA TCTCCATCCA GGAGCTGAGA ACCCTGCTGT CCGGGATTCT 2940
CTGCCATGGT CCCATAAGAC TAAAGGTTGA AGGCAAGTCC CTGACCCCTG CCCAGCTCCT 3000
CCCAGACACA GGCCAAGGCC CTAGTCCCTG AGGGCCATCT CAGCCAGGCA GGCCAAGCTC 3060
TGGATTGCTG GGCATGGGGG CTGTGACCCA CCCTCAGTCA CAGTCACAGA ACTGCCCCAC 3120
CCCCTGCCCC AAATCTGCAG CTCCCCAGTG AGATCACTGG AAATGAGGGT TGGGTGTCAG 3180
GGCCCGCTGC TCTCTGCCTC AGTTTACCTG CCTAAAGTGA GATGAACCAT CTTTGGCTGG 3240
GCTCTCTCAC TGAGACGGCC AATTGAGATA AGGCTGAAGA TGGCGAAAGC CCCACCACTG 3300
CCTGAGCACT TTCTGTGTGC CAGGCTCCCC ACGAGGTGGG ATGGCTTCCC CTTAGGGAGG 3360
TTACACACCC CACCCAAGGC AGCATGGCCA GGACGTAGCA GAGCTGGAAT TCAGACCCAC 3420
ACACCCTGGG TCCAGAGCAC ACGTGCTTAC ACGCTGAGCT ACGTGGTCAT CACTCAGCAA 3480
AGGGCCCCAT GTTCAGATCT GACTGGGGAG GCAGAGGGCA CAGCAAGTGG CAGACCCCCT 3540
GCCATGCTGG CAAACAGCTG CTGCACATCA CAGGGAAGCA TGCGCAGGGC CTGCAGGCAC 3600
CGGCTCCCGC GCACACGGAC CTGGAACACA CATGCTCACA CACATGCATG CACGCTGGGC 3660