EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS108-06373 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr10:105425220-105428360 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs3781339chr10105428152hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr10:105426075-105426094TGCTGCCCCCTGCTGGAAT-6.54
Tcf12MA0521.1chr10:105428252-105428263AACAGCTGCTG+6.32
ZNF263MA0528.1chr10:105426636-105426657GGAGAAGGGTGGGGAAGGGAG+6.63
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_01123chr10:105427529-105429036Adrenal_Gland
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
TTGGAAAGCA CAGACAGGCT ATGGCCTCTC TCAGGAGCTG CTCCAAAGGC TGTGGGATGG 60
ACACACGGAC ACTCTGTCCT TCTGGCTGCC CTTCCCTCCC GTTGCACAGG CAGGCTCCCA 120
GCTCTTCCCT CTGGCAGCTG CCTCTTAGGG TGTTCCCTGG CCAGGGCAGC CGGGCGGGCG 180
GGAGCTGCGA GCAGGTATCC AGATGAGAAA CCACTTGCAG GCCAGGCAGG CAGTGGGCGG 240
TGATGTCATC CCACAGAGGC CACTCTGGAT CCCCTCTCAG CCAAGGCCTG CAGAACTAGG 300
GGCTGGAGGA GTCTGCCTGA GTGGGGAGGG GGCAGTGGAG GGAGCCTGGT GTCTTTAGAT 360
GAGGAGTGCT TGGCAGGAGC ATGGAGAAGG GGTGTACCTC TTCTAGACAG CAGAGCCTCT 420
CCTGGGTTGG AAGGGGCCTT TGCATGAGTC TGATCCAGAG ATGGACCCTT GTGCTTTATT 480
ACAGAGCCCC TGGCTGGACC TGCTGGGGTC CCAGGGGTCC CCTGGACCCC TGCCCCACCC 540
TTGCCTCACA TCTGCATTCC TTCAACTACC ACCTGGATGG AACCCTGGCT GCCAACTTAA 600
ACTTCTCAAC TGGGCTTTTG CCAAGTCAGT CCCATGCTCC AACGCCTTCC ACGGCTCCCT 660
CTTGCCTATA AAGGACAAAT TCAAGCCCAG TCTTTCTTGC CAATCTGAGC TCCCCAAGTT 720
CCTTGATCCC CGTCCCCCAC ACCACCATTC AATACATCAT TCATGATTCA ACACATGTAT 780
CGAGCACCCA CTAGGCGCCA ACACCCAACA CCACTGCTCC ATGCAGCTTC TTACTTTCCA 840
AGTCTGTGCT CTAGCTGCTG CCCCCTGCTG GAATGCTTTC CCTTCTCTCT ACCAATCCCA 900
GTTTCCCAAT TCTCCCCAAG CATCTCTGTC CTCCAGGAGG CTCCTGATCA CTCTTGTTCC 960
CTCTTTTCTG TTCCCTCCTG GACTTTATGT TGGGCATTGC TCCCCAACCA AAGTATGTGC 1020
CTTGGACAAG AGTCTCTCGA CACTCCAGGA CTGGTGCCTC AGGACATGAC ATGGGACATA 1080
GTAATTACCT GAAATTCATG ATGGAAATGC TTAGAATTAG AGTCCAAAGG TCTGAGGTCC 1140
AGTCCTGCTT TGCCCTTACT AGCTCTGAGA TCCTGGGGAG GACACGTAAC CTCTCTTGAG 1200
CTTTAGTGTC ATCTGGAAAC AGGAACAATA GCAGTTCCTA CCTCATGGGA ATTGTTCTGA 1260
GCACGGAATG AAGTGACGGG GCTTCAAGTC CTATGGAAAT CATAGATGGT CATTTTAAAG 1320
CAAGTGGAGG GAATGGGAGA TCTGAGGAGC AGCAAAGCTG TTGGTTCCTT CGTGGGCTCA 1380
CCAGCAGGCA GCTCGGTGCC AGGGCTGCAG GTGCCAGGAG AAGGGTGGGG AAGGGAGGCC 1440
GGGGGCTGTG TCCCTGCAAC ATGCCCCTCC CAGACCCTAC CTTCAGCAGG TAACGGGTAC 1500
TTGCCAGCTG GATTGAGAGG CAGCTCAGAG CCCCCTGGGC CTACTCTGGG GGGATGCCAG 1560
GCTAAGCAAC CTGAGGCCCC TGATCTATAA GGATCTCCAA CATCAGCCCT TACCTCTGAG 1620
TTTCCTGTCT CATATCTCAA AGAACCCTCC AACCCTCCAG ATGGAGAAAC CAAGGCCCAG 1680
AGAGACTCTG GCCCTGGACT CGCAGTCTGG CTGGGTTTTC CCCCAGCCCA CACTGCCTCC 1740
CCTGGGCCTC TCACTCCAAA CAGCTGGGAT CATCTTGAGA CGTGGTTAAG TGTCCTCCCC 1800
AGGGTCACAG AGCTAGTAAG GCCCTGTGCT GGCCTCCACC CCAGGCTCCC CACGACTCCC 1860
CAACCCTGGG CATCCTACAA AAGTCCCTCT AGCCCCTTAT AACTGGTTCC TCCCAGGCTG 1920
GACTGGGACT GCTGGCCCCT CCGCTATACG TTTGGTGAAT AAAATGTATT GCTGTGGGCC 1980
AAGTGGGCTC TGGCTCACTG GCGTGTGGAG AGGGGAAAAA GGGACAGGAG CCCAGTGATT 2040
AGCTCAGGCC CAGGCCCTCG TCACAGGAAA CTCCAGAAGG AGATTGCAAC GCCCTCCGAC 2100
CCACTGCCTT CTCTTCTCCT CTGGACTCCT CCCAACACGT TTACCTCCCA TTCCCCGCCC 2160
ACAGCTGCAG CAGTAGGGGC TGGGCTTTGG GCTCTAAACA CTGGGGCTGG CCCAGCCCCA 2220
CCACCCCACT CAGCTCCCAC CCTTCTGCTT TGTCCCCTAT TCCCCCAGCC TGAACCTCTG 2280
CTCTCAGGTT TGGGGCTAGA GGGTCAGGGT GTGTAACAGC CTCAAAAATG GAGGGGTCCC 2340
ATAGAAGACC CTTCTGGAAA TTCCATCCCT CCTCCGACCA TCTCCATCCA GGAGCTGAGA 2400
ACCCTGCTGT CCGGGATTCT CTGCCATGGT CCCATAAGAC TAAAGGTTGA AGGCAAGTCC 2460
CTGACCCCTG CCCAGCTCCT CCCAGACACA GGCCAAGGCC CTAGTCCCTG AGGGCCATCT 2520
CAGCCAGGCA GGCCAAGCTC TGGATTGCTG GGCATGGGGG CTGTGACCCA CCCTCAGTCA 2580
CAGTCACAGA ACTGCCCCAC CCCCTGCCCC AAATCTGCAG CTCCCCAGTG AGATCACTGG 2640
AAATGAGGGT TGGGTGTCAG GGCCCGCTGC TCTCTGCCTC AGTTTACCTG CCTAAAGTGA 2700
GATGAACCAT CTTTGGCTGG GCTCTCTCAC TGAGACGGCC AATTGAGATA AGGCTGAAGA 2760
TGGCGAAAGC CCCACCACTG CCTGAGCACT TTCTGTGTGC CAGGCTCCCC ACGAGGTGGG 2820
ATGGCTTCCC CTTAGGGAGG TTACACACCC CACCCAAGGC AGCATGGCCA GGACGTAGCA 2880
GAGCTGGAAT TCAGACCCAC ACACCCTGGG TCCAGAGCAC ACGTGCTTAC ACGCTGAGCT 2940
ACGTGGTCAT CACTCAGCAA AGGGCCCCAT GTTCAGATCT GACTGGGGAG GCAGAGGGCA 3000
CAGCAAGTGG CAGACCCCCT GCCATGCTGG CAAACAGCTG CTGCACATCA CAGGGAAGCA 3060
TGCGCAGGGC CTGCAGGCAC CGGCTCCCGC GCACACGGAC CTGGAACACA CATGCTCACA 3120
CACATGCATG CACGCTGGGC 3140