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

TagContent
EnhancerAtlas ID
HS101-22007 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr19:45372800-45375100 
Target genes
Number: 41             
NameEnsembl ID
ZNF155ENSG00000204920
ZNF222ENSG00000159885
ZNF223ENSG00000178386
ZNF284ENSG00000186026
ZNF224ENSG00000186019
ZNF234ENSG00000263002
ZNF226ENSG00000167380
ZNF227ENSG00000131115
AC069278.2ENSG00000176761
ZNF180ENSG00000167384
IGSF23ENSG00000216588
PVRENSG00000073008
CEACAM19ENSG00000186567
BCL3ENSG00000069399
CBLCENSG00000142273
BCAMENSG00000187244
PVRL2ENSG00000130202
TOMM40ENSG00000130204
APOEENSG00000130203
CLPTM1ENSG00000104853
RELBENSG00000104856
CLASRPENSG00000104859
ZNF296ENSG00000170684
GEMIN7ENSG00000142252
PPP1R37ENSG00000104866
NKPD1ENSG00000179846
TRAPPC6AENSG00000007255
BLOC1S3ENSG00000189114
MARK4ENSG00000007047
CD3EAPENSG00000117877
FOSBENSG00000125740
VASPENSG00000125753
OPA3ENSG00000125741
EML2ENSG00000125746
SNRPD2ENSG00000125743
QPCTLENSG00000011478
FBXO46ENSG00000177051
SIX5ENSG00000177045
DMWDENSG00000185800
SYMPKENSG00000125755
FOXA3ENSG00000170608
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs395908chr1945373565hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxd3MA0041.1chr19:45373005-45373017GTTTGTTTGTTT+6.32
Foxd3MA0041.1chr19:45373009-45373021GTTTGTTTGTTT+6.32
ZNF263MA0528.1chr19:45373461-45373482TGAGGAGGGCGTGGATGGGGA+6.21
Number of super-enhancer constituents: 7             
IDCoordinateTissue/cell
SE_28236chr19:45371864-45374124Fetal_Intestine
SE_29374chr19:45372743-45374138Fetal_Intestine_Large
SE_31891chr19:45372886-45373850Gastric
SE_38686chr19:45372830-45374318HUVEC
SE_43252chr19:45372785-45373784Lung
SE_54232chr19:45372849-45374062Spleen
SE_65607chr19:45373251-45373809Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr194537286145374000
chr194537288745372981
chr194537305045373997
Number: 1             
IDChromosomeStartEnd
GH19I044868chr194537136345374450
Enhancer Sequence
GATCGCATCA CTGCACTCCA GCCTGGGCGA CAGAGCGAGA CTCCATCTCA AAAAAAAAAA 60
AAAAAAGAAA AGAAAATATG ATTAAGTGTA GGGTTTAATC AAGCCCAAAG CTTGAGGATG 120
ACCACCTGGG AGCATAGATT GAAGTTGCCC TGAATATACA CTTCAAGCAG GGGCCAAGGC 180
AAGCAGCTCT TGCAAGTGAG CTTTTGTTTG TTTGTTTGTT TCTTGGAGAG AGGGTCTCCA 240
AAACTACAAA TAAAAATTAG CTAGGAATGG TGGCGCACAC CTGTAATCCC AGCTACTCAG 300
GAGGCTAAGG CAGGCGAATT GCTGAAACCA GCAAGGGCAG GTTGCAGTAA GCTGAGATTG 360
CACCACTGCA CTGCATCCTG GGTGACAGCA AGACTCTGTC TCAAATTAAT AAAAAAAAAA 420
GAGAGAGAGA GAGATAACCT CAAGAGCTTC CGTATACACA CTGGTGCAGA AGTAAGGAAC 480
AAAACAGCCA AAGCCTCTGT CTTCATGATG CGTGAGCCAC CAAGGAATAG TTGGCCAGAG 540
TCGGCGGTCA GGAAAGTGCC CTTGACGAAG TGGGGCTTGG AGTGGGGTCT GGAGAAGGAG 600
GCCAAAGCAA TCCAGGCACA AAATCACCAA CCAAAACCCC AAAGTGGGTG GAGGCAGAGA 660
CTGAGGAGGG CGTGGATGGG GAGCATGTGG AGTGGCCAGG GGAGGTGGCC ATGGGGAAGT 720
GGTGGGCTCG GGCCCTGAGT CACTATTCTA ACAGCTTGGA GGGCGGCCAG GAGGATGTGG 780
GGAGGCTTGT TGGATGCTCC ACGATGGTCA GGGGAGAAGG CGGTGGGAAG GGAGAGCTGG 840
GAAGAAGAGG AGAGTCAGAC CGTGTTGAGA AGTTCAGAGG TGGATACCCA GGTCCAGAAA 900
GCAACAGAAG ATGTGAGTCT GGGTGGGGGA CACACATCAT AAGCATGAGC TGCTATTCTT 960
CCTGGAGTTT TGTTTTTGTG ATTTTTTTCC ATGTTTTCCA AGAGAATGAG GTGGAAAGGG 1020
TATAAAAAAA AGAAACGGCT TTGAGATTTT CTGCCTTTAT CACACTTCCA GTCATTCAAT 1080
CATCTAATGG TGATTACAGG AAAAGGAACA GGGGGCCTTT CCAGCTGGAC CTTTGAACCA 1140
CAGTACTCAG TTACTCGCTC GGCCTTGATT TGCTTTTTTT TTTTCCTTTT TTTTTTTTTT 1200
CTTTTGGAGA CAGAGTCTCA CTGTCACCCA GGCTGGAGTG CAGTGGCACG ATCTCGGCTC 1260
ACTACAACCT CTGCCTCCCA GGTTCAAGCA ATTCTCTTAC CTCAGCCTCC CGAGTACCTG 1320
GGATTACAGG CACCTGCCAC CACGCCCAGC TAATTTTTGC ATTTTTAGTA GAGATGGGGT 1380
TTCACCACGT TGGCCACGCT AGTCTAGAAC TCCTGACCTC AGGTGATCTG CCCACCTGGG 1440
CCTCCCAAAG TGCTGGGATT ACAGGCATGA GCCACTGCGC CCATCCTAAT TTTTGTATTT 1500
TCAGTAGAGA TGAGTTTTCA CCATGTTGGC CAGACTGGTC TCAAATTCCT GGCCTCAAGT 1560
GATCCACCCT CCTCAGCCTC CTAAAGTGCT GGTATTGCAG GTGTGAACCA CCACGCCCGA 1620
CCAGCTTTTT TTTAAATCTC AGCCTCCTCT AGGCTTTTGG ACCCTGTCTC TGCATCTCTG 1680
GCAGGGCGAA GAGACAGTAT ACCGAAATGG CCAGGCCAGG CGCCTGTAAC CTCAGAGCTT 1740
TGGGGAGCCG AGGTGGGAAG ATGGCTTGTG CTCAGGAGTT TGAGATCAGC CTGGGCAACA 1800
TAGCAAGAAC TCATCTCTAC AAAAAAATTT AAAAATTAGC CGGGCATGGT GGTGCATGCC 1860
TATGGTCCTA GCTACTCTGG AGGCCAAGGC GGGAGGATCA CTTGAGCCTA GGAGGTGCAG 1920
GCTGCAGCAA GCTATGATCA CACCACTGCA CTCGAGACCA GGTGACAGAG CGGGCCCCTG 1980
TCTCTAAAAA ATAAATAAAG TAAAATAAAA TGGGCAACAC TTGGATAGGG CAGTGCAGGC 2040
CAGACATTAC CCTAAGCCAT TTACCTATCA ATGTATTATT TAATTCACAC AGCAATCCTA 2100
GGGGTGGGTA CTTTCATTAT CCCCATTTTA CAAAACAAGA AACAGCTACA GAGTTGCAAA 2160
ACCACTTATC CCAAGCCAGG CCGCTGATAA GCAGCAGAGC TGGGATTGGA ACCCCGGCAG 2220
TTAGGGCCTA ACCACCCTGC TCCTCTGCTG AGTGTTTGTT GAATGACTGC CGGTGAGGAG 2280
TGACGCACCC CCTCTCCTCC 2300