EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS047-04841 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr10:105426020-105428360 
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: 26             
IDCoordinateTissue/cell
SE_01123chr10:105427529-105429036Adrenal_Gland
SE_04829chr10:105422511-105429995Brain_Cingulate_Gyrus
SE_05806chr10:105422432-105430177Brain_Hippocampus_Middle
SE_06868chr10:105427804-105429536Brain_Hippocampus_Middle_150
SE_07764chr10:105422452-105430753Brain_Inferior_Temporal_Lobe
SE_24302chr10:105427603-105428043Colon_Crypt_2
SE_24302chr10:105428076-105428522Colon_Crypt_2
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_41304chr10:105426389-105429198Left_Ventricle
SE_42617chr10:105426380-105429677Lung
SE_44236chr10:105427611-105429550NHDF-Ad
SE_44930chr10:105426679-105429496NHLF
SE_45960chr10:105425744-105429515Osteoblasts
SE_46694chr10:105426546-105427464Ovary
SE_46694chr10:105427582-105429072Ovary
SE_49112chr10:105425984-105429683Right_Atrium
SE_50307chr10:105426286-105429281Sigmoid_Colon
SE_52745chr10:105426640-105429718Small_Intestine
SE_65658chr10:105426429-105429179Pancreatic_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
ACACCCAACA CCACTGCTCC ATGCAGCTTC TTACTTTCCA AGTCTGTGCT CTAGCTGCTG 60
CCCCCTGCTG GAATGCTTTC CCTTCTCTCT ACCAATCCCA GTTTCCCAAT TCTCCCCAAG 120
CATCTCTGTC CTCCAGGAGG CTCCTGATCA CTCTTGTTCC CTCTTTTCTG TTCCCTCCTG 180
GACTTTATGT TGGGCATTGC TCCCCAACCA AAGTATGTGC CTTGGACAAG AGTCTCTCGA 240
CACTCCAGGA CTGGTGCCTC AGGACATGAC ATGGGACATA GTAATTACCT GAAATTCATG 300
ATGGAAATGC TTAGAATTAG AGTCCAAAGG TCTGAGGTCC AGTCCTGCTT TGCCCTTACT 360
AGCTCTGAGA TCCTGGGGAG GACACGTAAC CTCTCTTGAG CTTTAGTGTC ATCTGGAAAC 420
AGGAACAATA GCAGTTCCTA CCTCATGGGA ATTGTTCTGA GCACGGAATG AAGTGACGGG 480
GCTTCAAGTC CTATGGAAAT CATAGATGGT CATTTTAAAG CAAGTGGAGG GAATGGGAGA 540
TCTGAGGAGC AGCAAAGCTG TTGGTTCCTT CGTGGGCTCA CCAGCAGGCA GCTCGGTGCC 600
AGGGCTGCAG GTGCCAGGAG AAGGGTGGGG AAGGGAGGCC GGGGGCTGTG TCCCTGCAAC 660
ATGCCCCTCC CAGACCCTAC CTTCAGCAGG TAACGGGTAC TTGCCAGCTG GATTGAGAGG 720
CAGCTCAGAG CCCCCTGGGC CTACTCTGGG GGGATGCCAG GCTAAGCAAC CTGAGGCCCC 780
TGATCTATAA GGATCTCCAA CATCAGCCCT TACCTCTGAG TTTCCTGTCT CATATCTCAA 840
AGAACCCTCC AACCCTCCAG ATGGAGAAAC CAAGGCCCAG AGAGACTCTG GCCCTGGACT 900
CGCAGTCTGG CTGGGTTTTC CCCCAGCCCA CACTGCCTCC CCTGGGCCTC TCACTCCAAA 960
CAGCTGGGAT CATCTTGAGA CGTGGTTAAG TGTCCTCCCC AGGGTCACAG AGCTAGTAAG 1020
GCCCTGTGCT GGCCTCCACC CCAGGCTCCC CACGACTCCC CAACCCTGGG CATCCTACAA 1080
AAGTCCCTCT AGCCCCTTAT AACTGGTTCC TCCCAGGCTG GACTGGGACT GCTGGCCCCT 1140
CCGCTATACG TTTGGTGAAT AAAATGTATT GCTGTGGGCC AAGTGGGCTC TGGCTCACTG 1200
GCGTGTGGAG AGGGGAAAAA GGGACAGGAG CCCAGTGATT AGCTCAGGCC CAGGCCCTCG 1260
TCACAGGAAA CTCCAGAAGG AGATTGCAAC GCCCTCCGAC CCACTGCCTT CTCTTCTCCT 1320
CTGGACTCCT CCCAACACGT TTACCTCCCA TTCCCCGCCC ACAGCTGCAG CAGTAGGGGC 1380
TGGGCTTTGG GCTCTAAACA CTGGGGCTGG CCCAGCCCCA CCACCCCACT CAGCTCCCAC 1440
CCTTCTGCTT TGTCCCCTAT TCCCCCAGCC TGAACCTCTG CTCTCAGGTT TGGGGCTAGA 1500
GGGTCAGGGT GTGTAACAGC CTCAAAAATG GAGGGGTCCC ATAGAAGACC CTTCTGGAAA 1560
TTCCATCCCT CCTCCGACCA TCTCCATCCA GGAGCTGAGA ACCCTGCTGT CCGGGATTCT 1620
CTGCCATGGT CCCATAAGAC TAAAGGTTGA AGGCAAGTCC CTGACCCCTG CCCAGCTCCT 1680
CCCAGACACA GGCCAAGGCC CTAGTCCCTG AGGGCCATCT CAGCCAGGCA GGCCAAGCTC 1740
TGGATTGCTG GGCATGGGGG CTGTGACCCA CCCTCAGTCA CAGTCACAGA ACTGCCCCAC 1800
CCCCTGCCCC AAATCTGCAG CTCCCCAGTG AGATCACTGG AAATGAGGGT TGGGTGTCAG 1860
GGCCCGCTGC TCTCTGCCTC AGTTTACCTG CCTAAAGTGA GATGAACCAT CTTTGGCTGG 1920
GCTCTCTCAC TGAGACGGCC AATTGAGATA AGGCTGAAGA TGGCGAAAGC CCCACCACTG 1980
CCTGAGCACT TTCTGTGTGC CAGGCTCCCC ACGAGGTGGG ATGGCTTCCC CTTAGGGAGG 2040
TTACACACCC CACCCAAGGC AGCATGGCCA GGACGTAGCA GAGCTGGAAT TCAGACCCAC 2100
ACACCCTGGG TCCAGAGCAC ACGTGCTTAC ACGCTGAGCT ACGTGGTCAT CACTCAGCAA 2160
AGGGCCCCAT GTTCAGATCT GACTGGGGAG GCAGAGGGCA CAGCAAGTGG CAGACCCCCT 2220
GCCATGCTGG CAAACAGCTG CTGCACATCA CAGGGAAGCA TGCGCAGGGC CTGCAGGCAC 2280
CGGCTCCCGC GCACACGGAC CTGGAACACA CATGCTCACA CACATGCATG CACGCTGGGC 2340