EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS045-09429 
Organism
Homo sapiens 
Tissue/cell
Fetal_lung 
Coordinate
chr10:104371180-104373280 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL2MA0478.1chr10:104371466-104371477CTGAGTCATCC-6.32
JUNBMA0490.1chr10:104371466-104371477CTGAGTCATCC-6.14
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_00121chr10:104368529-104374374Adipose_Nuclei
SE_01828chr10:104370197-104371987Aorta
SE_01828chr10:104372043-104373418Aorta
SE_03928chr10:104370718-104373779Brain_Anterior_Caudate
SE_04957chr10:104372139-104373712Brain_Cingulate_Gyrus
SE_05850chr10:104370353-104374026Brain_Hippocampus_Middle
SE_06794chr10:104371996-104373907Brain_Hippocampus_Middle_150
SE_13930chr10:104371206-104373827CD34_Primary_RO01536
SE_26660chr10:104370849-104372002Esophagus
SE_26660chr10:104372101-104373893Esophagus
SE_28107chr10:104372056-104373197Fetal_Intestine
SE_29332chr10:104372053-104373036Fetal_Intestine_Large
SE_29601chr10:104371986-104373965Fetal_Muscle
SE_31097chr10:104371927-104373686Fetal_Thymus
SE_31421chr10:104372228-104373868Gastric
SE_38034chr10:104369989-104374139HUVEC
SE_42120chr10:104370475-104372035Lung
SE_42120chr10:104372147-104374145Lung
SE_48604chr10:104370331-104371938Right_Atrium
SE_48604chr10:104372092-104374133Right_Atrium
SE_50092chr10:104370376-104372089Sigmoid_Colon
SE_50092chr10:104372093-104374101Sigmoid_Colon
SE_51270chr10:104370062-104371939Skeletal_Muscle
SE_52411chr10:104371007-104371986Small_Intestine
SE_52411chr10:104372048-104373580Small_Intestine
SE_53301chr10:104371297-104373451Spleen
SE_54642chr10:104370759-104372088Stomach_Smooth_Muscle
SE_55138chr10:104372231-104373364Thymus
SE_62334chr10:104369841-104439105Tonsil
SE_65286chr10:104370147-104374252Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr10104371223104373182
chr10104372653104372974
Number: 1             
IDChromosomeStartEnd
GH10I102610chr10104370284104374099
Enhancer Sequence
CCAGTGGTTG ACCAAAGCCT GCAGGGTCCA CTCAAGGAGT CAGGAGCTCT TTCAAGCCCC 60
ATCTCAGAAG TACCCTCTCC CAAGCTCCAG GCAAGAACCT TTGTTCAGCA GGGAACTGGC 120
CTGGCCAGAG GCAGTTGTAA AGGCAAACAA GTTTTGGTTA AGCCATTGAC ATTTTTACAG 180
GAGGAGCAGA TAGACTTTTA GAGGCAGCCA GCTAACGTCA ACACATTAAT GCACTTGTCA 240
GATATATTGT GAGCACCTAC TACATCCCAG GCACTATTGG CCTTATCTGA GTCATCCCAT 300
TTAGTCATAA TGACCTATTG TTATTTATTC TTGTTAAGAG GATACCAAAG CCCAGAGAGA 360
AGTTAAGCCC AATGTCACAT AAAACTGGAA CCCAGAACTT AAGCTGTTAG CCACTCTGCC 420
TCCTGGAGCA CAGCCTTGGC CCCATGCCCC TGGCAGTCCC CAGCGGGTAT GAGCTGTGCC 480
TCCCTGAGAG CCCCTCTCCC TTCCAGCCCC CAAAGCCATG CCTTCCCCTC CACTGGGAAC 540
TCAGGGAGAA AACAGCCCAG CTGAAAAATT AGGCCATGCT GCCGAGCACA CTACTTATTT 600
TTTATGACTA AGATTAAGCT GACAACCATG CAAAACATTG CAAACCTGTG TCGGCTGCAG 660
ATTTAATACC TCACCTAGCC CACACAAATA ATTCATGCTT CTGCATCGAT GTCCAGAAGA 720
AACAAATCAG CAGAAAACTG GGTTCTTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG 780
TGTGTGCACG CGCATGTGTG TGTGTGTGTA TAGCAGCCGC GTTTCCATCG AAGCAGCATG 840
CCGGAAATAC CCAAGCTCCA GGACTGCAAA TCTTGCATTT TGCAATTTTT TTTTCTCTTA 900
AAAGATTAAA GTACAGTTTC AAATGATTGA AGGTTGGTGG GAGGTGTAAA TGTGGGCACT 960
TGTCACATTA ATTCTTCAGA TGATTAAGTT CTTTTCCATT TCTTTAAGGC TGTTTGCAGT 1020
TGGGTTTGAT GTCCTGGTTC TGGGTGAGTG TGTTGTGGCA GTTACCAAGG TGACTTTAGC 1080
TGACTTTCAA CAATTTATTT TTCCCTCCAG CTTGAGACGT CTCTAGCCCT GTGTGCTGTT 1140
GATTCTTTTC TGCAAGCCCC CACCCCACCT CCCATTGCTA TTCATGAGCA TTTTTGCCTG 1200
CACCATAGAG GCTGGGATTC TCTAGCACGC CCTGCCTGGA CAAGCTAGGC CTCAGCCCCT 1260
CTCAGGAGGA CAGTAGTGTG TCTGGAGGCA GGAACCGGTG GTCAAAGATG GCACAGGGGA 1320
GTGATTGTGA GAGTCACCCC CTGGTCCTTT CGCTTAAACT CACTCTGAGC CCTTCGGCTC 1380
GTCACCTCAC CTCCCTAAGC CTCAGTTACC TCCTCTGTGA AAGAAGGCTT GACAACAGAG 1440
CCTACCTCGT GCTTGCTGGG AGGAATCAGC GAGTGAACCT ATGGCCTTAG CAGAGGGTTG 1500
GCGCAGAGTA AGGGCTCAGG AAACATGGCT CAGGAAACAC TGCTTCCTGA GTTCTGCTCT 1560
TGTTTGGGCC CTGAGGGCAC CCTATGTCTC CACTGAGCCC TCACCTGTGA CTGCTGCCTC 1620
CCTCAGAAGG AAGGGAGGTG CAGTGGCCCT GGTGGAAGGG AAAGAGAGTT GGTCGGAAGT 1680
CTGAGGCTTC GATCAGAAGT CTGACGCACG GTGAGGGGGG ACGCGTCACC CACTCTCTTT 1740
TGTAAAGGAA AGAGGGAGAT TAAACAACCT CAGAGTTTCC TTCCAGTCCT GAATACTGTG 1800
ACCCTCTTGG CCATAGCATT TGTCTCCTTC ACAGGTCTTG CGCAAAGGCG AAGCCAGGGG 1860
AAAAGGCAGT TTTAGAGCTG GCTTTAGGAA AGCAGAGGAA GGGACCGCTT TGTGAAGGAA 1920
CAGTCAGATC CAGGAGTGAG TCCTCACAAG GAGAAGGCCA GCAGGCAGGC ACGGCCCATG 1980
ACCTCAGGGG CACGTCTAAC CCACTGCCGC CACAGGGCCA TCCTCTGTCT TTGGCCTGCG 2040
GACCCTACAC CTTCCCCTGG GGAGGTGCCC TGCCTGTTGG GGTGCCACCC TGGCTGCAGG 2100