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

TagContent
EnhancerAtlas ID
HS069-04430 
Organism
Homo sapiens 
Tissue/cell
GM18951 
Coordinate
chr19:45224200-45229420 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs150820726chr1945227155hg19
rs7254776chr1945227742hg19
TF binding sites/motifs
Number: 11             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GATA2MA0036.3chr19:45228160-45228171TTCTTATCTTC+6.02
IRF1MA0050.2chr19:45229339-45229360TTTTTCTTTTTCTTTCTTTTC+6.31
IRF1MA0050.2chr19:45224654-45224675AAAAAAAAAAAGAAAGAAAAA-6.59
IRF1MA0050.2chr19:45224771-45224792ATTCAGTTTCTTTTTTTTTTT+6.71
Nr2f6(var.2)MA0728.1chr19:45226395-45226410GAGGTCAGGAGTTCA+6.22
Nr2f6(var.2)MA0728.1chr19:45225175-45225190TGAACTCCTGACCTC-6.22
SPI1MA0080.4chr19:45225788-45225802CAAAAGGGGAAGTG+6.41
SPIBMA0081.2chr19:45225790-45225802AAAGGGGAAGTG+6.07
ZNF263MA0528.1chr19:45226881-45226902GAAGGAGGAGTAGGAGAGATG+6.2
ZNF263MA0528.1chr19:45228451-45228472TCCCCCTCCGCCCGCTCCTCT-6.62
ZfxMA0146.2chr19:45226371-45226385GAGGCCGAGGCGGG-6.01
Number of super-enhancer constituents: 19             
IDCoordinateTissue/cell
SE_09606chr19:45225026-45227473CD14
SE_23197chr19:45226609-45227960Colon_Crypt_1
SE_23197chr19:45227985-45229989Colon_Crypt_1
SE_23877chr19:45226698-45227829Colon_Crypt_2
SE_23877chr19:45228030-45229465Colon_Crypt_2
SE_26699chr19:45226534-45229277Esophagus
SE_31568chr19:45225186-45226205Gastric
SE_31568chr19:45227174-45229356Gastric
SE_34750chr19:45225301-45226193HeLa
SE_34750chr19:45226424-45229782HeLa
SE_47531chr19:45228001-45229336Pancreas
SE_53360chr19:45224892-45226462Spleen
SE_53360chr19:45226521-45227795Spleen
SE_53360chr19:45227895-45229537Spleen
SE_56197chr19:45227061-45227913u87
SE_56197chr19:45227922-45228447u87
SE_62704chr19:45221152-45271677Tonsil
SE_65330chr19:45224918-45226537Pancreatic_islets
SE_65330chr19:45226619-45230111Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 6             
ChromosomeStartEnd
chr194522843645228775
chr194522676045227161
chr194522544145225906
chr194522464745224919
chr194522862845228743
chr194522527445226089
Number: 2             
IDChromosomeStartEnd
GH19I044722chr194522426445224919
GH19I044721chr194522504145229949
Enhancer Sequence
CAAATTATCT TAACAGACAT TTCTCAAAAG AAGACGTACA ATGGCCAACA AGTATATGAA 60
AAAATACTCA ACATCATACT CATTGGGGAA ATGCAAATCA AAACCACAAT GAGGTATTAT 120
TTCACCTGAG TTAGGATGGC TGTCATCAAA AAGACAAAAA ATGGCCAGTT GTGATGGCTC 180
ACGCCTGTAA TCTTAGCACT TCGGGAGGCC GATGTGGGCG GATCACTTGA GGTCAGGAAT 240
TCGAAACCAG CCTGGCCAAC ATGGTGAAAC TTCAACTCTA TTTTTGTAAA AATACAAAAA 300
TTAGCCAGGC ATTGTGGTGC AAGCCTGTAA TCCCAGCTAC TCAGGAGCCT GAGGCAGGAG 360
AATCACTTGA ACCCAGGAGG CAGAGGTTGT GGTGAGCTGA GATGGCGCCA TTGCGCTCCA 420
GCCTGAGCAA CAGAGAGAGG TTCCCTCTCA AAAAAAAAAA AAAAAGAAAG AAAAAAAAAA 480
AAGGAGCAGG GATTCAGCTT TGAGGGCCAT GGCGAGGATT TTGGCCATCA CCCCAAGTGA 540
AGTAGGAGCC ACAGAGGCTG GATGGGTTCT GATTCAGTTT CTTTTTTTTT TTTAGATGGA 600
GACTTGCTCT GTCGCCCAGG CTGCAGTGCA GTGGCGCAAT CTCGGCTCAC TACAACCCCC 660
GCCTCCTGGG TTCAAGTGAT TCTCCTGCCT CAGCCTTCCC AGTAGCTGGG ATTATAGGCA 720
TGTGCCAACT CACCCAGCTA ATTTTGTTGT TGTTTTGTTT TGTTTTGTTT TTTGAGACAG 780
AGTTTCACTC TTGTCTCCCA GGCTGAAGTG CAATGGTGCC CACTCAGCTC ACTGTAACCT 840
CTGCCTCCGG GGTTCAAGTG ATTCTCCTAC CTCAGCCTCC TGAGTAGCTG GGATTACAGG 900
CATGCACTAC CACGCCAAGC TAATTTTTGT ATTTTTAGTA GAGACGGGGT TTTGCCATGT 960
TGGCCAGGCT GGTCTTGAAC TCCTGACCTC AGGTGATCCA CCTGCCTCAG CCTCCCAAAG 1020
TGCTAGGATT GCAGGTGTGA GCCATCATGC CCGGCCCTGA TTCAGGTTCT AACAGGATCC 1080
CTCTGGCCAT GAGGTGGAAA GAGACTGTTG GGGGCAGAAT TGTAAAGCGA GGGACAAGAA 1140
GAGTCAGGGG TCTCCAAGCT TTGAGCCTGA GCCACTGCAA GGATGAAGCT GCCATTTCTG 1200
AGGCCAGAAG GCTGCAGGCA GGGCTGGGTT GGAGATTGGA ATGAAGATAG GTCTTGTTTG 1260
AGGCCAATGA GGAGGGAGCC TCACCCGAGG CACACAGGCT CCAGGCGGGA AGTTGGCGAC 1320
AAGTTGTGGA CTGTGGTTTT CACCCACCTC ATGGGGCCCC CTCATCCTCT CCCCCAACTT 1380
CCCCTCACGC CGTGGTGGAG CCAGCTTTGT TTGTTTCCCC CCCATCATCC GTTTCATGAT 1440
GGGGAAGACT GGTTTTCCCC TAACCCAACA GACACCTCTT CCCTCAGCCT GTCCCTGACC 1500
CTCCCACCTC GGGAAGCCCC GAGCGGGCCT CCCAGAATGT CCCGGCAGGA AGGGGCTGCT 1560
GCTACCGTTC ATCCAGCCAG ATGAACCCCA AAAGGGGAAG TGGGTCACCC GTAGTCACCC 1620
GGCTCATGGT CAGCTCGGGA CTTCAGGATC TCGTCTCTTC ACTGCACCCA CCACAGCCCT 1680
GGGAGGTTTT CCATGCACGC TTCTCATTCT CCCCACATTT CACACGAGAA AACAGGGGCT 1740
CCAAGAGAGG CCCACACTCA CCTAAGGAGC TCGAAAGATA GGGGCATCTG GATTTGAACC 1800
CAGGTCCTAG CAGATGTTGT TAGCTCAGAG GAGAAGGCAG AGAGGGTGAA CAGAACCCAG 1860
CCTGCCCTCC CAGATCCAGT GGGAAGGCAG ACTTGTCCCC AGGTAATAAT AGCCCAGCAG 1920
TGTTCACAGC CTGGGATGGA GGAGCCCAGG AGGCTGCAGG AGCTCAGAGC GCATGCCTGA 1980
CCCAGCCTGG GGTCAAGGAG GGCTTCCTGG AGGAAGGGAC AGCTCATCTG ATACCTAGAG 2040
GATGAGTGGG AGTTACTAGG TGTAAATAGT GCAGGGAGAG GGAAGAGTAT GTGCAAAAGC 2100
CTAGGGTTGA GAGGAAACCT AGGGGCTCCA GCAAGGCGCA GTGGCTCATG CCTGTATTCC 2160
CAGCACTCTG GGAGGCCGAG GCGGGCGGAT CATCTGAGGT CAGGAGTTCA AGACCAGCCT 2220
GGCCAACATG GTGAAACCCT GTCTCTATTA AAATACAAAA ATTAGCCAGG CGTGGTGGCG 2280
TGCACCCATA ATCCTAGCTA CCTGGCAGGC TGAGGCACGA GAATTGCCTG AACTTGGGAG 2340
GTAGAGATTG CAGTGAGCCA AGATCACGCC ACTGCACTGG CGACGAAGTC AGATTCCATC 2400
CCTCTCTCTC AAAAAAAAAA AAAGCTGGGG GGAGCCTAGG GGCTTCTAAA TCCGATCGTG 2460
TCCTGGCCCT GATTAAACTC TCCTACAGCT GCCCTGGCAA ACTCTTTAGC TTGGCATTCA 2520
TTCATTCATT CATTCATTCA CTCATTCATT CCATAAACAT TCCCTGGAGT GCATTGTCAG 2580
TGTCAGGCCC CAGGGGAACA CAGCAGTGAC CACGACAGCC CCACCAGACC ATGACCCTGA 2640
CCAGGGGGCT CACGAGGGCG GAGACATCTA CTCCAAGACC TGAAGGAGGA GTAGGAGAGA 2700
TGCTGGGGAA GAGGCAGGGA AGGGTGTTCC TGGCAGAGGG AACAGCCTGT GCGAAGGCCT 2760
GAAGGTAAGT TTTGCATATG ACACCTTTGA GAAACTACTT ATTGTTCAAC TGAAGCATAG 2820
GGTTGTTCAG AAGAAGCCAG CCTTGTGGCC GGGTGTGGAC TTCCTCCCAG GGCACCAGGG 2880
AGCCACTGCA GAGTTGTGAG CAAGGGACAG ACAGAGGTAG GCTTGTACTT CCAAGAGACT 2940
CCCCCAGCTG CCACATGCAG GGTGAATGGA ATGATGCACA GAATCCAGTT TCAGGGGTAG 3000
TTTGGTACTT GGACCCAGGT CCCAGGGAGA GAGTCCAAGG AGCCCTTCTC TGGTCTTCCA 3060
AGGAGCTGCT CTCCCCAAGC TCCGGATGGA AGGCGTGCCC ATGGCAACCG CTAGGTGGTG 3120
CCCGTACACC ACCAGCCAGG TCTTTTTTTG CCAAAAGTAG ATCAGGCCCA GAGCTGGGCA 3180
GAACTGCCCC TGGGTCAGGA GAGCAAATCG TCTCTGTCTT TTGGTCCTGG CTCCCTGGCC 3240
AGGCATCCTG GGGCCATTTG ACTCCCAGGC TCAGGAAGGA GCTGGCTGAG CTGCAGTGAG 3300
TATGTTCTTC GTCTCTTTCC TCACCTTGGA ATCTCAGACG GGAGCACCCT GGCTCCCACT 3360
TCAGACAGGA AGATTCTTAC CTCCCTCATC AGACTAGCAG GCTCTTTGTC TCCCCACCAG 3420
TTTGAGGGGC TCCCCATTTC TATCATTCAT TTGGAAGCTC ATCAGCTCTC CCAGAAGGCA 3480
TGGGAGCCCT TCAACACCCC CATCAGACTA GGACTACCCA TCTCCCCCAT CAAATTAGAA 3540
CTGCATTGTC TCACACATCA AAGTATCACT CCTGGCCAGG TGCAGTGGCT CCCGCCTGTA 3600
ATCCAAGCAC TTTGGGAGGC CGAGGCAGGA GGATCACCTG AGGTCAGAAA TTCAAGACAA 3660
ACCTGGCCAA CACGGTGAAA CCCGGTCTCT ACTAAAAATA ACAAATTAGC CAGGCGTGGT 3720
GGTGTGCGTC TGTAATCCCA GCTACTCAGG AGGCTGAGGC AGGAGAATCG CTTGAACCCA 3780
GGAGGCACAG GTTGCAGTGA GCCAAGATCA CACCACTGCA CTCCAGCCTG GGCGACAGAG 3840
CGAGACTCTG ACTCACAAAA ATAAATACAT TGTCTTACAC ATCAGAATGT TGCTCCTTAC 3900
CTCCCCTGGC AGACTGGAAA TATAGACTGG ACACTCGTTC TTGCTGCACA GGACTGGAGC 3960
TTCTTATCTT CTTCATTGGA TTTGGACAGT CCTGTCTCCC TCATGGGATT TGGTGAGAGC 4020
TCCTTAGTTT CCTTATTTTT CCCACTGTGT TGGGCCACCT TGTCCCCACC ATCAGATTGG 4080
GGAACACCTT GTCTCCCAGT CAGACCAGAG GGGCGGACTC CTCTGCCCTT GCAAAGGTTC 4140
CTAGGTCCTT CTTACATCCA TAGGAGGAAC CATGCCTATT TTACCAAGAG GGAAACTGAG 4200
GCACAGAGAA ACAAAGCACC ACTTCTCTGT CCAGCTGCAG ATGCCTCCAC CTCCCCCTCC 4260
GCCCGCTCCT CTGCCCCTGC CCTCCCCCGC CCCCGCCCCT GACCTGGGTA ACTCCCCTGG 4320
CACCGGGAGT AGGGGAATTT TGCCCTGCTG GCCTCTGCAC CAACCACCTC CCCTTATCGG 4380
CAGCGTCGCC ACCAGTGGCG GCCCAGGGTT AAAGTCCGGA GAGAGCTCCG GGCGCGAAGC 4440
GGATAGGGAG GGAGGAGTGG CGCCCAACCC AGAACGGGGA CTCCCCGGAG GTCGAGCCCT 4500
CACGCTGCTG GGAGGAGAGG GGATGGGCAG GGCCGTGTCC CATGGTAAGG TGTGGGTTCA 4560
ATCCTTCCTT TCTAGTTCCC GGCTGTGTGG TCTTGAACCT GGAACTTCAC CCCAACTGGG 4620
AGCCTCAGCT TCTCCAGCTT TAAGGAGTCA GGGGCGTGAA AATGTCCAAG CTCTGGAGTC 4680
AGACTCCAGG AGTTTGAATG CTGGCTCCTA TAACCTGCTG TGTGAGATCT GGGGCCAGCG 4740
AGTGTGTCTC TCTCAGCCTC AGTTTCCCCA GCTGTGCAAT GAGGATACCT AGTGGGTGGT 4800
GGTGAACGCT CCATGAGTTT ACGCACAAGA AAACCTTGGG ACAGTGGCTG ATAGTGGCGC 4860
CAGCAAGCCA GCATGCACCC CACCCTTTCC TTCCAAGAAA ATTGCCTCCT AAATCTATGA 4920
TTGGTAACCT TCACCCCTCC CTCTTTGACC CACCTCCTAA CCCAGGCCAC CTGGTGTCTT 4980
GCTGCACAGC TGGTCTCCCT GCCCGCACCA CACCCAGAGG CGTCCTTGGA AACCCAACCC 5040
TGACCCCTGG TCAGAATCTG CCATGGCTCC CCAGTGCCCC CAGGAGAAAG CCAAGTGCTG 5100
TGCCACAGCC ACAGCCTGAC CACTCACTGC TTGTATTTTT TTTTCTTTTT CTTTCTTTTC 5160
TTTTCTTTTT CTTTTTTTTT TTTTTTTTTA AGACAGGGTC TTGCTCTGGC CCCAGGCTGG 5220