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

TagContent
EnhancerAtlas ID
HS179-15007 
Organism
Homo sapiens 
Tissue/cell
SkMC 
Coordinate
chr17:76403130-76406050 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs4129767chr1776403984hg19
rs4969143chr1776405736hg19
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HES2MA0616.2chr17:76403233-76403243GGCACGTGCC+6.02
HES2MA0616.2chr17:76403233-76403243GGCACGTGCC-6.02
NR2C2MA0504.1chr17:76403352-76403367AGAGGTCAGAGGTCA+8.73
Nr2f6MA0677.1chr17:76403353-76403367GAGGTCAGAGGTCA+7.42
RREB1MA0073.1chr17:76403141-76403161TGGGTGGTGTTGGGTCGGGG-6.78
RxraMA0512.2chr17:76403353-76403367GAGGTCAGAGGTCA+6.88
TCF3MA0522.2chr17:76405422-76405432AGCAGGTGTT-6.02
ZBTB18MA0698.1chr17:76404983-76404996ACACATCTGGATG-6.78
ZNF263MA0528.1chr17:76405178-76405199CTCTCTTCATCTTTCTGCTCC-6
Number of super-enhancer constituents: 18             
IDCoordinateTissue/cell
SE_00336chr17:76403376-76405707Adipose_Nuclei
SE_06227chr17:76402742-76404378Brain_Hippocampus_Middle
SE_09402chr17:76402394-76405762CD14
SE_18476chr17:76402170-76405866CD4p_CD25-_Il17-_PMAstim_Th
SE_24583chr17:76402500-76404137Colon_Crypt_2
SE_24583chr17:76404346-76406027Colon_Crypt_2
SE_26825chr17:76402621-76404160Esophagus
SE_26825chr17:76404693-76406004Esophagus
SE_31461chr17:76404354-76405962Gastric
SE_36965chr17:76401030-76406003HSMMtube
SE_42104chr17:76403056-76404193Lung
SE_42104chr17:76404335-76406043Lung
SE_45620chr17:76403242-76404276Osteoblasts
SE_50905chr17:76402998-76406411Sigmoid_Colon
SE_51088chr17:76403004-76406193Skeletal_Muscle
SE_51835chr17:76403263-76404154Skeletal_Muscle_Myoblast
SE_53161chr17:76403031-76406409Small_Intestine
SE_63627chr17:76403263-76404226HSMM
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr177640354176404103
chr177640532976405828
Number: 1             
IDChromosomeStartEnd
GH17I078406chr177640281476406178
Enhancer Sequence
CTGCCCTGGT GTGGGTGGTG TTGGGTCGGG GCGGGGGGTG CCCTGCAACC CAGGAGTGCT 60
GGATGAGTGG GAAATTGGGG ATGATCTTAC AGCTGGATCC CAGGGCACGT GCCCATGTGG 120
GGGATGGGAT TGGGGGAGAG TTGGCAGAGG TGGGTGAGGG ATGGATGGTG TGTGGAGGGG 180
GCTGCTGCTG AGCAGAGGGG CTTCACCCTA AAGCCAGGAA CCAGAGGTCA GAGGTCACTT 240
GATGCTGAAG TGAGAGGCGA GGGTCCTTCC CTGCTCAGTG GTTGTGTCCC CAGTGGGATC 300
TTAAGTCAGC ACCTCTTCAG GCCCATCTTT TGATGGTCAC TTCCTCCAGG GCAGCGTGTG 360
TCAGGTGAGA GATGAGTGGG CAGCCGCAGG GTGCTTGTGG ATTTCGATGG CTGGCCCAGT 420
GGACCATTCA TTTCCTGACT GTCTGCCCTT TGCAAGGCAC TTGCTGGGTA CAGGCTCTGT 480
GCCTCCTTGG GTGTGTCTGT GTTTGGGCCC CAGAAAATTC CTGCCGGTGG CTATGCACTG 540
ATACCTCCAC TCCCTTACTC AGGTCCTGTA GGACAGGCCT GGGCTGATCT CAGCTCCTCC 600
TGCTCCCAGA AGCCCTTGGG CAGAGACAGG TAGCCAGGAC TCTGTGGATT CTAGATCCTT 660
GCCCCTCAGA CAGCACTCTG CTGTCAGCAC AGCACTCTCT GGGAGCCAGG CAACAAGAGG 720
CTTCACGGAG TGACTGTGTT GAACTTGCTG GTGGCCCCAT GAGTGTGGTG ATGCAAGGAA 780
GAGCAGCGTG GGGGGAAGAG GCACCTTCTC ATGTAAAATG ACCCCGTGGC TCAGCAGCTG 840
CCAGTGGATT TCAGTGCAGT CTGGTGACAG AAAATTCAGA GGGCTGGCCT TTATTCTTAA 900
GGGTTTTCTG TGTTGTCAAG TATTGCCAGG ACTGTCTGGC AGTTGCTTAG ATGCCTTGTT 960
GGAAAGATTC TTGTGTGATA ACCATTTGCC GATCGTTCAA CAGCCTGATA CACCTCTTTT 1020
GCATACTATG CTGATTTCTT AACATATTTT ATCTATCAAT CAGTCAATCA GTCTATCATG 1080
TATCTCTATC ACATTTCAAT AAATTGAGCT GTTTCAAAGA ACCAGAGGAA CACTCAACTA 1140
TTTAAAGGCA TGCACTAGAG ACTTCTTTTG CAATATGGTT TATCTATTTC ATTCTTATTT 1200
GGATTTTTGT AAAGGGTGCC TATTCAGAAT ACTCAGGAGA AGCCATGCAA GTGTGATTTG 1260
GCATAGGGAT TACTAGACTT GAAGTCTAGA AGCCTGGTTC TGAGTCCACA TTTACCTGTG 1320
GCCACAGCTG AGGGGCCTGG CTTAACCTCT TTCCTGTGCA GTCGGGGGGA TGGCTCTAGA 1380
TTGTCAGGAG GACACGGGGA ACAGGGCTGA TATTTGACTT TCTATAAAAT AACCGTATGG 1440
TTCCTAGGCC AGGTGAGGCA CCTTGGTGGG GCGCGTGGAG GTTGAAATCA CACTGGGGGC 1500
CGAGGGCTGC TGCGCGTCCC TGAGCGAATA GATTGGCAGA AGGGAGTGGG GTGGGGGCCT 1560
TGGATCCCTT GGTGCCGTGT CTCTGGCCTT GCTCCCTGTA GTTCTGTTGC GCTGATTCGG 1620
TCGTGAAGGA AGGTGCTGCC AGGCCGCTTC ACCTGCATCG CCTTGGCTTT GGGAGGTGGG 1680
GCTGAGTGGG CATCTGGGTT GGATCTCAGG CAGGTGGCAG TTCCTCTGAT TCATGGTTGT 1740
CAGTTTCCTG TTGCCTGGCC CTCGCTCCTC GCCCAGTAGG TGTGGTGGGA CAAGGTTCTG 1800
GGAGCTGGGG TAGAATTTGG ACTCTTAACG GGAAGTGCCT CGTGCTGCCG CAGACACATC 1860
TGGATGGGTG CTGAGCTTTC CTTCCCAAGC CTGGTCCTGA TCGGGGGTGG GGTACAGGCA 1920
GGAGCAGCCC GGCCTTGTCA GCCGTTGAAA GTGTGGTATC TGCTGGGTTG CCAGTAAGCT 1980
CGCTTCGAGG TCTTGAGAGG CAGTGCAGGG GAGGCTGAGT ATGAACCGTG TCAAGCCAGT 2040
TCTTATGTCT CTCTTCATCT TTCTGCTCCA TGGAGGTGAG GGACAGAGTG AGTGGTGCCC 2100
ATCCCATTAT CACATTCAGG CAGGAACCAT GCTGTGCTGA GCCAGGCTGT GTCCATCTGC 2160
TGGGACATGG GCTCTGCCCT CCGGCGTGCA TTTCATGAGG AAGATCAGAA AGTGAGTTTT 2220
AGCATGTTGA CTTCCATTTC TTCTGGACGC AGTATTCTAG CACTAACAAC ACAATGTGGG 2280
TGGCTAGGGC GGAGCAGGTG TTGGATTAAG AGATTTCTGG CTCATGCTGA CAGGGAAATC 2340
TGTTAATGGT TGTGAGAATG TCACTATTTT TATTGCCTTC CTGATAGGCC AATTGGCGTT 2400
CTGCCCAAAG GTGAACTGAT GGTGAGAGGC GGGCAGCCCC ACCCTGTTTG CCTAGGCCAC 2460
ACGTGAGGCG GCTCTCCCCT GGGCACCCAG TGGGTGTGGT AGGGGTGCTG TGCCCGTGCA 2520
AATTGCTTGC TTCAGGCTGA GCACACACAC CAGCCTGTGG GCCCTTACAG TTTCTCAGAG 2580
CTGTACTAAT GTCAGAGCAG GTGAGTGCTT ATCCTGTAAG GATAAGCCTG TGATGTCTTC 2640
TGTCCCCTCC GTGTTTTTAC TGGAGTCTGA GAACCCTGTA AGATTTATTG CAGAATACTG 2700
TGGGAGTGCT TGAGGGAGGA GTATGTGTTC ATGCATGTAC TCTTAAAATG TTCATACACT 2760
TCTGCCTTAG AACTGCAAAG GCCTGGCGTG GTGGCTCACA CCTATAATCC CAGCACTTTG 2820
GGAGGCCAAG GTAGGCGGAT CACCTGAGGC CAGAAGTTTG AGACCAATCT GGCCAACATA 2880
GTGAAACTGT GTCTCTACTA AAAATACAAA AATTAGCCGG 2920