EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS177-21709 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH_RA 
Coordinate
chr7:116151440-116153150 
Target genes
Number: 11             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
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: 1             
ChromosomeStartEnd
chr7116152142116152412
Number: 1             
IDChromosomeStartEnd
GH07I116509chr7116149154116154310
Enhancer Sequence
TGTACCTGAA ATGCTGCCAT TGGAACTTGA CATCTTGATA CTTTTTTAAG TGAAACACAC 60
CCTTGAGTGG GGTAACATTT CAATCTATTA GCAGTCATCT ATTTACTTTA GGTGAACAAG 120
TGATCTGAGA AAGGAGTGTT GAAAACTACA TATGGGAACC AAGCATAAGA GCTCTGAGCA 180
CAATATGAGA GCACCATACA CTGATTAAAA GAGATGTCAC CAAAGAGAAA GCTGTGACAA 240
AGGGAAACAA GAGGCTCCAA TCACATGGCC TTCAGCCTTC CCAGTTTCGC TTTTGGACAA 300
CCCAAATCCC TAGTGAAAGG GGCATGGAAT CTGAACAGGA GTGGAGGAAA TTGAAGTCAG 360
CTAAAGACTT TTCTTTTTAT CCACAAAGGA AAGTTGCTTT TGTCTTACTG AATGAATAGG 420
ACCCTAGGAG TGGGCATGAG GGCTCTGCTG GAACCATGTG CCCTAAAGAC AATGCCGAAG 480
CGTGCAACTG AAAATGAAAA TGAAACTGTA ACTTGTGACC ATCTATCTGT GTCTTCTTTC 540
GCCTTGCCTC TCTGTGCTGT TGACTGTTGC GGCATGTCTG CGGCAAAGAA AGACCATGCT 600
GCAGTCAGAG AAATCAGAGG ACACCACTTC AACAATTAAC CAAAAATAGG ACAGGGACAC 660
CTATCTGCCT GTGCTTGGAC GTATTAGGTC ATTCAGCTCA GCTGTGTGAC TGGAGAAATC 720
ATTTTGCCTT TATAGGAAAA GGTAGGGGTG TAGGATGATG AGAGAAAGGA AGAGACATGA 780
CTCAGAGTGG GAAACAGCAC GTAGCCAAGG GCAAATATTT CTCTCAGACA TAAATGGATC 840
AGGAAGAGGT GAGAGCAGCA GGTCATCTTT GGAGCATTCT TTTCTTTCCT GCCTCCCAGT 900
CACTTGTCAC CGAGCACCAA CCAGTAACAA AAGGGGAGAG AAGGGCAGTA TGCAGGACCT 960
GTTTCTCTAA CTGACTGGCA CATCGGTTCC AGCCAACTGC TGTCTCAGCT AACTAGGGCA 1020
GTGAAACAAG GAGTCATTTG GAAAGTTTCA GGGATGCACA CTCCACATCG CAGGGAGGCA 1080
AGTGGTGAGG AATAACCACC ACGCTTATTT TACTGAGGAG GAAACTGGTT GAAATTCTTT 1140
ATGTATTATA TGGCTGGGAG ACCTCTGATC TCAGTACAAA CAATAACAGG AGTATTTAGA 1200
TTTGTCGAGC ACTTATAATC TTCTGGGCAT TTACTTAATC AGTACAATAA CCCTACGATG 1260
GGAATGTTAC TGTCATTCCC ATTTTTCAGA TAATGAAACT GATGCTGTGA AGTTAAAGAA 1320
TTTGCCCTAG ACCACAGTCA GGATGTGAGC CAAGAGAGCC TGACATCAGA GCCCACACTC 1380
CTAATCACTG TAGAGATGAT TTTCTATTTC CTGAAAGAAT GTGTCCATGG CTGTTCTTAT 1440
GGCTTCCAGC CAAAATCTTC TTTTTTCATT CATCCACCTT TCCTACTCTG AGAAGCACCT 1500
TTTTTTCCAT TCTCCCATCA ATGGAGGCAG TTTCATGTCC TCAGTTGTAA GAGCTGTCCC 1560
AAGCTAGCAC CTGGGCTTCA TGTAACCTCC TCACTCGGCC TCCATCTAAT CCCTGAACCC 1620
CTCCCCCAGC CCTGTATGCC GCTTTTCAGG GCACACCCTT TCTTTCTCCT TAGGATCTGA 1680
GCTCTAGACC TTACACTCCA GCTAAAGTCA 1710