EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS176-17294 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chr17:73686850-73689510 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs820218chr1773687495hg19
rs820217chr1773688294hg19
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_03279chr17:73686303-73692257Brain_Angular_Gyrus
SE_04001chr17:73682465-73705208Brain_Anterior_Caudate
SE_05218chr17:73683487-73704230Brain_Cingulate_Gyrus
SE_06028chr17:73679436-73705327Brain_Hippocampus_Middle
SE_07212chr17:73682397-73698116Brain_Hippocampus_Middle_150
SE_08211chr17:73682578-73702695Brain_Inferior_Temporal_Lobe
SE_08990chr17:73686664-73687322Brain_Mid_Frontal_Lobe
SE_08990chr17:73687443-73688040Brain_Mid_Frontal_Lobe
SE_08990chr17:73688788-73689532Brain_Mid_Frontal_Lobe
SE_24278chr17:73687432-73687807Colon_Crypt_2
SE_26294chr17:73686877-73691992Duodenum_Smooth_Muscle
SE_26940chr17:73683620-73687341Esophagus
SE_26940chr17:73687344-73688470Esophagus
SE_26940chr17:73688670-73693050Esophagus
SE_31090chr17:73682484-73690062Fetal_Thymus
SE_31632chr17:73688999-73690686Gastric
SE_33907chr17:73688424-73692522HCC1954
SE_34296chr17:73687618-73698150HCT-116
SE_34660chr17:73686212-73700594HeLa
SE_35907chr17:73679249-73694632HMEC
SE_37434chr17:73687394-73694818HSMMtube
SE_38365chr17:73679204-73691897HUVEC
SE_41082chr17:73687344-73697964Left_Ventricle
SE_42678chr17:73687803-73697989Lung
SE_49201chr17:73687983-73692681Right_Atrium
SE_49763chr17:73688739-73690995Right_Ventricle
SE_50776chr17:73686217-73698254Sigmoid_Colon
SE_52592chr17:73686851-73698261Small_Intestine
SE_53680chr17:73689060-73690952Spleen
SE_55482chr17:73683668-73688641Thymus
SE_56442chr17:73685734-73692981u87
SE_64300chr17:73679247-73688655NHEK
SE_64300chr17:73688895-73693069NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr177368740273688371
chr177368839273688688
Number: 1             
IDChromosomeStartEnd
GH17I075683chr177367912573698792
Enhancer Sequence
AGGTATAGCC AGCAGGAGGC AGATTCCCAG ATTGATTCTC CAGAGCCTTG TAGGTCCCAA 60
GGGTGCCTAT GACACCAATG GGAATCTGAA CCAACACAGA CAGCACAGTC TTCTTAGGAG 120
ACCCTAGTGC AGCAGCGCTG GCCTCCTCCT GAGCGTGCAC GCTTATATGG CTTCTGAGCT 180
GGCCAGGCTA CTTCATGCAT TTGGTTTAAT GGGTCCTCGT AAGGCAGGAG AATCTTCTTG 240
AACTTGGAGT TGGGTCTGTG GTCCATTGGT CAGTACTTTG TTCAGAGGCA CTGAGGGTGG 300
GAAGGCTCAT GGAGCTGGAT TCTGCTGCTG GGAAGCTGGG TGGGCCTTGT TTGTGGGCCT 360
CAGGTTCAGG ACTGAATGAG AGTCCTCTTG TTGCGAGTTG AGGGTGTACT CTGGGCATGC 420
CATGCCCTTT TTTTGTACTA AGAGGGTAGA AAAGCAAAGA CCAGACTAGT TGGCAAATTG 480
GAACCCAACT ACCCAGTTTA TTTATTTCTT AGGCGTAGAA GGAATAATTT AGGGGGAACT 540
GAAGAGCCAA CCTAAAGGAA AAAAATAAAA TAAAGGGATA AAATACTTCC TGTGATTTTG 600
CCCCATCATC TCTTTTCTTC CAGAGACGTG ACTCAACAAC CTCAGCTGAG CCTGGCAGCA 660
CACACACCCC ACACTCCTTT CCATCTCCAG GTTCACAAAA GCCACAAGAA GCCACGGGGA 720
GGCTCCTGGC CTCTTACTTT ACCTAAGGAG GCCCTGAAGT GGCAAGTGTG TTTCCCCTTG 780
AAGAGCCATT GCATGTTTGG TGACTAACTT CCTGTGGCTT TGGGGTAGAC ATGGTAGACT 840
CCTTGTGTGG GGATTGGGCC TCTGCAGTTG AGTCCATGAG AAGGGGTGGG TGTGGTATGG 900
TGCGGAGCCT TGGGGAAGGG TGAGTGGGGG CTGGAGGGAG AGTTAACGAA TGGTCAGTCC 960
CTGTATGATC AGCCAGCTGG CGGGTGAGGG AGGAGCTGAT GTTTTCCTAC AATCAGCACC 1020
CAGAAAGCTG TTCTCTAGAG GGAAAATGTG AGGGCATTTT ACAGTCCCAT GTATTGTTAC 1080
TAACACTCTT GAACACTGGT TTCCTGAGAG TCACTGCTAC AAAGGGATTG TTGGTCCCCT 1140
GAGAGACTGG CAGTCTCTAT AGGGCTGCTG ATTTATGACT GCGGCAGTCT CTATAGAGCC 1200
GCTGATTTAT GACTGCAACC TGAAGTTGGT GTGGCAGTCC TCCAGGCGCG CCTCCCTGCC 1260
TGCTCCCAGC CTCCTCTTTG CCCACCTGAT TGGCAGGGGG CAGTGGCTCG AAGAGATGGG 1320
TTGCTAAGCA GCCTGGCCTG GACGTGGTGC CCTGCCAGGT TGAATGAATA GCTGCAGTGT 1380
TCTGAGGAAT GGGGAATTTG GCCTGTCCCA GCATCAGGAG GGACTTTCTG GAAAGGGGGC 1440
TAAGACTGAG TCTAGGTTCA GTGTGGGGAA CTGGGTGGCC TTCCTGGCAC CTTCCTTTTG 1500
GAGCCGTGGC GTGGTGTGCC ATGTCTGTGT AAGTGGAGCC TGCGGAGCTC TGCACCTGTC 1560
CTCGAAAAGG TCTTGTTGCA GGGTCTTCCT GTCTCATCTC CTCCCTCACT CATCAGCAGG 1620
AAAAGACATG GCGTCCAGCA ACTTTCTGTG AACTCTGCCT CTGCTGTTTT GATGATGAGC 1680
ACGTGTGGCC CTTGAGATTG TTGATCTAAC TGGCTTTGAG GGGCTGGGTG TCAGCAACCC 1740
AGAAATGGGG GAAACAGGTG TGTTCTTGCC ATTTTACACT TGAGACAATG GAGGCAAGGG 1800
AAGACTTGTG ACGGAGGGCT TGGACCGTGG CTTTCTCAGC ATTGATTTTG GTTTAGATGA 1860
AACATTTACT ACAGAACAGT GAAATCCAGA AAACGTCTAA GAAGCCTTTG CTCTCAGGTT 1920
TCTGCAGGAC ATGTGGATGT AGCTGTCATG GGACACTGTT TGCATTAGGG ATTGGAGGAA 1980
GCTTTTCTTT GGAGGGAGTA TAAAGCCAGT GTAAAGGGAG CTGAGAGCCA GAGAGAGGCT 2040
TCCTTGAGCC TGGGGCCTCT CTGGGATCCC CATTCTGCCA CTTATTAAAG GTTTGCTGCA 2100
TGCTTGCTCT GAGGTTCCAT GAGCTGCCCC TTTATCCTCA TGATGAAGCC TCCCTTCTTT 2160
GAACTAAAAA TAAGAAGAGT ATCTTGGGAG CAGCTAGTCT GCATTTTCAT CTCGGGAGTC 2220
TGCTGTTACA AAGCAGTCAC CTCTTGCTTC CTTGGTACCA GCGGTAGAGG TGGTGATGTC 2280
TGGGCTGGCC GGGCCCTTGA GCTCTGCACT CCATTCAGGC AAGCTTCCTC AGACCCAGGG 2340
GAGAGCAACA GGCAGGGTAT ACGTTGCCCA GTTGGCTGCA GCAGGCTTGC TGGCTTGTGT 2400
TCTCCTCAGC GATGGTGGGT TTGGTCACTG AAAAGGCATG GAGGAGAGAC CGGCGTGGGG 2460
CTCGGGAGCA TCCGGCTGCT GCGATGCGGG AAGAAGAGGG TTCGGAGGCT CGGGGGTGCC 2520
AGAGGCCCCT GAAGCATCAG CTTACCCTTA GTGTTCCTGG CAGTGCTTTT ACTTTTTCTC 2580
CTTCCTTAAA AATCCTGAGT GGTCTCAGTA GAGAGTAGCT GGTTCAGGAG CCCCAGTCTT 2640
ACCTCCTCGT ATTTGTTTGT 2660