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

TagContent
EnhancerAtlas ID
HS101-22011 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr19:45382200-45385460 
Target genes
Number: 44             
NameEnsembl ID
ZNF155ENSG00000204920
ZNF222ENSG00000159885
ZNF223ENSG00000178386
ZNF284ENSG00000186026
ZNF224ENSG00000186019
ZNF234ENSG00000263002
ZNF226ENSG00000167380
ZNF227ENSG00000131115
ZNF233ENSG00000159915
ZNF235ENSG00000159917
ZFP112ENSG00000062370
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: 7             
IDChromosomePositionGenome Version
rs41290120chr1945382675hg19
rs406456chr1945382717hg19
rs3852860chr1945382966hg19
rs11669338chr1945382984hg19
rs11673139chr1945383037hg19
rs406315chr1945384116hg19
rs79701229chr1945384931hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RREB1MA0073.1chr19:45383434-45383454CACCCACCCACCCCACCCGG+6.16
ZfxMA0146.2chr19:45384693-45384707GAGGCCGAGGCGGG-6.01
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_43252chr19:45382840-45383849Lung
SE_54232chr19:45382777-45383842Spleen
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr194538439545384686
chr194538265945383074
Number: 1             
IDChromosomeStartEnd
GH19I044878chr194538141145383222
Enhancer Sequence
GGTGTCTTGT AATACATCAG ACCCCCTCCT TGCATGTTGG GGAAAGAGAG GGTGGGACAG 60
GGACTCCTAG GTCCCAGGGC TGGGAAGAGC TGATCCACGC CCCCGGGGAA CGAGAGCCTG 120
GCAGGGGTTA GACTGGGGAA GGCTGTGGGG CTCGGACCAC TTGGATCCTT GAAAGACGCA 180
TTGGATGGCC GAGAACCGCA AGGCTCGTGC AACTAGGATT CAGGTCACTG GATTGGGGAC 240
TCAGAGGCCT GGACATTTGG ACTCCTGGGT CCCAGGACAG AGGCTGCCTT TCTGGATGGT 300
GTGGCCAGAC CCATCAGAGG CAGGAGTTCT CTGGACTCCT GGGCCCTCGG GTGGAGGTGG 360
GGGTGGGGAC AGCAGGGGCT CAGCCAGGTT CCCTGCGTCC TGAGAGAATG AGGCCAGAGG 420
GCTGTGATCC AGTGGAGCCT CAGACCTCAA CTCCCCCAGG TTGCTGGGGG TCTCGGGAGG 480
GGAGGGCTGC TCCCCACTCC CATTCTTAGG GGCCCTGAGG GCATGGGGCA GGCGGGGGGT 540
GCTGGGGAAG TCCCACCTCT GGCCACCCCG ACTGTGGCTC CCCTCCTTCT CCATCCTTGC 600
CCCCAGGGAT CACCCCAGGG GACTTTTCAG TGGCTCCCTG GGAGTGGCGG CAGCTCCCTC 660
CAGCTCCTCT CAACTGGAAA AGCAAAGACG GGGGGAGGGG CGGCCCTTGG TCCTTGAACT 720
CCCAGGCTCA GTAAGGGACA GGTTTTTACC CGCGTCACCT CTGCTCTCCC AAGCCTCCAT 780
GCCTCCTCTG TAACACGGGG CAGGTGTTTC CATCGGCCTC ACAAGGCTGT CGTGGGACCC 840
AGTAAGGACA TGCCCGTGAT GCCCTCATGC AGCCTCATTG ACCTCCACAG ACCCCACCAA 900
GCCCTGTGCC AGGCAGTGCT GGGGCTGCAG CTGTGGCCTG CACAGACCCA GTGCCGTCCT 960
CCGGTGTGCA CGGCCATAAT GACCACAAGA ATAGCAGCAG TATGTTTAGG ATGAAGGTGT 1020
GTGTGTGGAC CGAGGGGCAG TCTCTCTCTC TCACTCCCCC ACCCTCTGAA GCCCTCCAGA 1080
GGATGCCAGG CTGTGGAACG GGAGCAGTGG AGATCCAACA GTCCAGCGTC CTCTGGAAGC 1140
TTCCTCCTCA TCTGGAGAGT GAGGCCGATG CATGCGTGAC CCCCACGGGC CCTTCCATAC 1200
TTGTTACTTC CTCTGGTTGT TTGTTGTCTG TACTCACCCA CCCACCCCAC CCGGACAACC 1260
GGAGGGCAGG GGCGGGGAAT TGGGTCCGCC TGGCACACAG TGGATCCTTC AGTGCCATGC 1320
TGAGTCCTCC TTACACACCC AGCAAACACC TACTGTGTGC CGAACCTCAG GCACACAGTC 1380
TAGTATGGAA ATTGGCAAGT AAACGGGTAA CCACTCCAAA AACTCTTCCA TTAGGAAAGA 1440
CTTGAGAAAT GGAAACGGGA GGTGCTAGCA AGGAAGGAGA GGCCCAGGAG CAAACAGGCT 1500
TCTCGCTTCT CGACCCCTTT TCCTGTCTTG CCTTTTTTTT TTTTTTTTTT TTTTTTTTTT 1560
TTGAGACGGT GTCTAGCTCT GTTACCCAGG CTGGAGTGCA GTGGTACGAT CTCGGCTCAC 1620
TGCACCCTCC ACCTCCCAAG TTCAAGCAAT TCTCCTGTCT CAGCCTCTTG AGTAACGCAC 1680
CCAGCCTTTT TTTTTTTAAG AAGTGGGGTG GTCTCCCTAT ATTACCCAGA TTGGGCTCAA 1740
ACTCCTGGGC TCAAGCGATC GATCCTCCCA CTTCAGCCTC CAAAAGTGCT GGGATGACAG 1800
GTGTGAGTCA CTGTGCCTGG CCCCTGGCTA ATTTTTTTTT TTTTTTTTTA AGACGGAGTT 1860
TCACTCTTAT CCAGGCTGGA GTGCAATGGC GCGATCTTGG CTCACGGCAA CCTCCGCTTC 1920
CCAGGTTCAA GCAATTCTCC TGCCTCAGCC TCCTGAGTAG CTGGGATTAC AGGCGCGCGC 1980
TAGCATGCCC AGCTAACATT TTGTATTTTT AGTAGAGACA GGGTTTCTCC ATGTTGGTCA 2040
GGCTGGTCTC AAACTCCCAA CCTCAGGTAA TCCACCTGCC TCGGCCTCCC AAAGTGCTGG 2100
GATTACAGGC GTGAGCCAAC GCGCCCGGCT AGCCCCCGGC TAATTTTTAA AATTTTTTCT 2160
AGAGATGAGG TCTTGTGCTC GTTGCCCTGG CTGGTCTTGA ACAATCCGCC CGCCTCGCCC 2220
TCCCAAAGCG CTGGGATTAC AGGCGTCAGT CACTGCCCCA AGCCCTAACC CCCTTCCTGA 2280
TAAGTGGAAG GAGATTCTAG TCCCCAGAGG TGATTCTGGA TCCCAGAATT CTGTCCCCGC 2340
ATTCTCTGTC TTCTAGCCGC CCCTGGTCCT GTCTCCTCTC CTCTCATCTT CCCACTCTGC 2400
CCCGCCTCAT TCTGCCCCAG CTACACAGTC TACTTGCTGT TCTTTAAAAA CAATACAAGG 2460
CAGGCCGAGC ACGGCATAAT CCCAGAACGT TGGGAGGCCG AGGCGGGAGG ATCACTTGAG 2520
CCCAGGAGTT CAAGACCAGC CTGGGCAACA TGGCAAAACC CCATCTCTAC AAAAAAATTC 2580
AAAAAAAAAA AAAAAAAGCT GGGCCTGGCG GCACATGCCT GTAGTTCCAG CCACTCCGGA 2640
GGGTGAGGTG GGAGGATCGC TTGAGCCCAG GAGATTGGGG CTACAGTTGG TGGTGATCAT 2700
GCCACTGCAC TCTAGCCTGG GTGACAAAGC GAGACCGTCT CAAAAAAAAC CATAGAGCCC 2760
CACAAGCCTC CTGCAGGGCC GCTGGCTGTT TGCGCTGCCT GCGATACCCC CAGACACTCT 2820
CATGACTCAT CCCCGGTGTC TCTTTCAGGC CCTTGCTCAG TTGTCACCTT ACAGTAAGGT 2880
AGAGGCCCTC CCACTACCTT CGGGGACCCC ACTTTGCACC TCCTATCACT TCCGCACTGT 2940
ATATTTTTGT ATCCCCCGTG ACTTACTCCC ATCTGGCATG TGAGCTATTG TACTGGTTTG 3000
CTTACTGTTG TTCTCCCTGC CCAACCAGAA TCAAAGTTCC ATGAAGGTAG ACACTTTGTA 3060
TGTTTTGTTC TCCACTCATC TCCCATGCGG GGCACACATC CTCGCTCCTT CCTCATGCTC 3120
AGCAGTTTGA GTTGAATGAA AGAATGTCCC CTGCCCATGG GAGAGGACAT AGACAGGCAG 3180
GCGATGATGT GGGGTGGGAT GGTCGCTTGG AATAAGGAGC TGTGGCTTCC TCCTGGAGAC 3240
CCCCTCACGC TGTCCCTCTC 3260