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

TagContent
EnhancerAtlas ID
HS101-41273 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr7:116151060-116153230 
Target genes
Number: 9             
NameEnsembl ID
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs10281637chr7116151338hg19
rs2024211chr7116153025hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr7:116151924-116151945CAACTGAAAATGAAAATGAAA-6.44
IRF1MA0050.2chr7:116151930-116151951AAAATGAAAATGAAACTGTAA-8.15
IRF2MA0051.1chr7:116151934-116151952TGAAAATGAAACTGTAAC+6.11
IRF9MA0653.1chr7:116151932-116151947AATGAAAATGAAACT+6.03
ZNF263MA0528.1chr7:116152192-116152213GGATGATGAGAGAAAGGAAGA+6.09
Number of super-enhancer constituents: 26             
IDCoordinateTissue/cell
SE_00018chr7:116129016-116153530Adipose_Nuclei
SE_02161chr7:116151581-116152636Aorta
SE_02523chr7:116151299-116153326Astrocytes
SE_25999chr7:116150746-116153480Duodenum_Smooth_Muscle
SE_34370chr7:116150806-116155330HCT-116
SE_35952chr7:116150008-116153550HMEC
SE_37708chr7:116150718-116153503HSMMtube
SE_38167chr7:116149533-116154406HUVEC
SE_40752chr7:116150991-116153288Left_Ventricle
SE_42280chr7:116151093-116153290Lung
SE_44303chr7:116151069-116153343NHDF-Ad
SE_45399chr7:116151448-116152740NHLF
SE_45690chr7:116149731-116153519Osteoblasts
SE_47185chr7:116148763-116156528Panc1
SE_48749chr7:116151357-116153221Right_Atrium
SE_51703chr7:116151100-116152857Skeletal_Muscle_Myoblast
SE_54095chr7:116151332-116153225Spleen
SE_54603chr7:116150962-116153355Stomach_Smooth_Muscle
SE_55667chr7:116150637-116154078u87
SE_63491chr7:116151064-116152929HSMM
SE_64530chr7:116150866-116153213NHEK
SE_67473chr7:116150637-116154078u87
SE_67977chr7:116101587-116180485TC32
SE_67978chr7:116101587-116180485TC32
SE_68523chr7:116131780-116168629TC71
SE_68524chr7:116131780-116168629TC71
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr7116152142116152412
chr7116151142116151209
Number: 1             
IDChromosomeStartEnd
GH07I116509chr7116149154116154310
Enhancer Sequence
CAAGTGCTTA CAGAATTTTT ACAGGGTTAC ATGTTACTTT AAGAAACTTA AAAAAATAGT 60
AAGTAGAGCT GCAAAGAAAA ATTACCACAA TGAATGTAAT TTATCACAAA TCAGGATTTG 120
GTACACTTCT TCCCTTCAAG TTGTGTATGT GTGCAGGGAA GACAGGGGAA GAAGTTGACA 180
GAGGAGGAGT AAAGGATACA GGTATACTAG ATAGTCAGTT TATATTTTTT AGGAATAAAA 240
ATAAGTTTGG CAACTATAAT TTAACCATCC CAATTTCTTC TCCCTATTCA CCCCAAAATA 300
GCAAAATGAG CAAAATAAAG CACCCCTTGC TAAATTTTTA AGACATTTCT GTGCCCACTC 360
TCCAGTTTCT TGCTTTGGAT TGTACCTGAA ATGCTGCCAT TGGAACTTGA CATCTTGATA 420
CTTTTTTAAG TGAAACACAC CCTTGAGTGG GGTAACATTT CAATCTATTA GCAGTCATCT 480
ATTTACTTTA GGTGAACAAG TGATCTGAGA AAGGAGTGTT GAAAACTACA TATGGGAACC 540
AAGCATAAGA GCTCTGAGCA CAATATGAGA GCACCATACA CTGATTAAAA GAGATGTCAC 600
CAAAGAGAAA GCTGTGACAA AGGGAAACAA GAGGCTCCAA TCACATGGCC TTCAGCCTTC 660
CCAGTTTCGC TTTTGGACAA CCCAAATCCC TAGTGAAAGG GGCATGGAAT CTGAACAGGA 720
GTGGAGGAAA TTGAAGTCAG CTAAAGACTT TTCTTTTTAT CCACAAAGGA AAGTTGCTTT 780
TGTCTTACTG AATGAATAGG ACCCTAGGAG TGGGCATGAG GGCTCTGCTG GAACCATGTG 840
CCCTAAAGAC AATGCCGAAG CGTGCAACTG AAAATGAAAA TGAAACTGTA ACTTGTGACC 900
ATCTATCTGT GTCTTCTTTC GCCTTGCCTC TCTGTGCTGT TGACTGTTGC GGCATGTCTG 960
CGGCAAAGAA AGACCATGCT GCAGTCAGAG AAATCAGAGG ACACCACTTC AACAATTAAC 1020
CAAAAATAGG ACAGGGACAC CTATCTGCCT GTGCTTGGAC GTATTAGGTC ATTCAGCTCA 1080
GCTGTGTGAC TGGAGAAATC ATTTTGCCTT TATAGGAAAA GGTAGGGGTG TAGGATGATG 1140
AGAGAAAGGA AGAGACATGA CTCAGAGTGG GAAACAGCAC GTAGCCAAGG GCAAATATTT 1200
CTCTCAGACA TAAATGGATC AGGAAGAGGT GAGAGCAGCA GGTCATCTTT GGAGCATTCT 1260
TTTCTTTCCT GCCTCCCAGT CACTTGTCAC CGAGCACCAA CCAGTAACAA AAGGGGAGAG 1320
AAGGGCAGTA TGCAGGACCT GTTTCTCTAA CTGACTGGCA CATCGGTTCC AGCCAACTGC 1380
TGTCTCAGCT AACTAGGGCA GTGAAACAAG GAGTCATTTG GAAAGTTTCA GGGATGCACA 1440
CTCCACATCG CAGGGAGGCA AGTGGTGAGG AATAACCACC ACGCTTATTT TACTGAGGAG 1500
GAAACTGGTT GAAATTCTTT ATGTATTATA TGGCTGGGAG ACCTCTGATC TCAGTACAAA 1560
CAATAACAGG AGTATTTAGA TTTGTCGAGC ACTTATAATC TTCTGGGCAT TTACTTAATC 1620
AGTACAATAA CCCTACGATG GGAATGTTAC TGTCATTCCC ATTTTTCAGA TAATGAAACT 1680
GATGCTGTGA AGTTAAAGAA TTTGCCCTAG ACCACAGTCA GGATGTGAGC CAAGAGAGCC 1740
TGACATCAGA GCCCACACTC CTAATCACTG TAGAGATGAT TTTCTATTTC CTGAAAGAAT 1800
GTGTCCATGG CTGTTCTTAT GGCTTCCAGC CAAAATCTTC TTTTTTCATT CATCCACCTT 1860
TCCTACTCTG AGAAGCACCT TTTTTTCCAT TCTCCCATCA ATGGAGGCAG TTTCATGTCC 1920
TCAGTTGTAA GAGCTGTCCC AAGCTAGCAC CTGGGCTTCA TGTAACCTCC TCACTCGGCC 1980
TCCATCTAAT CCCTGAACCC CTCCCCCAGC CCTGTATGCC GCTTTTCAGG GCACACCCTT 2040
TCTTTCTCCT TAGGATCTGA GCTCTAGACC TTACACTCCA GCTAAAGTCA GAAAAATAGT 2100
TCCCAAATGC CATTATTCTC ATTTTTTGTA AATTTTGTAG CATTTTATTC CTTCACACAG 2160
ACTTCCCTAA 2170