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

TagContent
EnhancerAtlas ID
HS091-12602 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr14:24547310-24549310 
Target genes
Number: 44             
NameEnsembl ID
NGDNENSG00000129460
AP1G2ENSG00000213983
DHRS2ENSG00000100867
AL136419.1ENSG00000197775
DHRS4ENSG00000157326
DHRS4L2ENSG00000187630
C14orf167ENSG00000215256
RP11ENSG00000225766
LRRC16BENSG00000186648
CPNE6ENSG00000100884
PCK2ENSG00000100889
DCAF11ENSG00000100897
NRLENSG00000129535
FITM1ENSG00000139914
PSME1ENSG00000092010
FAM158AENSG00000100908
RNF31ENSG00000092098
PSME2ENSG00000100911
RN5S383ENSG00000199804
IRF9ENSG00000213928
REC8ENSG00000100918
IPO4ENSG00000196497
TSSK4ENSG00000139908
TM9SF1ENSG00000100926
CHMP4AENSG00000254505
AL136419.6ENSG00000260669
MDP1ENSG00000213920
NEDD8ENSG00000255526
GMPR2ENSG00000100938
TINF2ENSG00000092330
TGM1ENSG00000092295
RABGGTAENSG00000100949
DHRS1ENSG00000157379
C14orf21ENSG00000196943
LTB4R2ENSG00000213906
CIDEBENSG00000136305
LTB4RENSG00000213903
ADCY4ENSG00000129467
NFATC4ENSG00000100968
NYNRINENSG00000205978
KHNYNENSG00000100441
CBLN3ENSG00000139899
SDR39U1ENSG00000100445
CMA1ENSG00000092009
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs743271chr1424548567hg19
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RFX1MA0509.2chr14:24549049-24549065GGTTACCATGGAAACT+6.45
RFX1MA0509.2chr14:24549049-24549065GGTTACCATGGAAACT-6.46
RFX2MA0600.2chr14:24549049-24549065GGTTACCATGGAAACT-6.78
RFX2MA0600.2chr14:24549049-24549065GGTTACCATGGAAACT+6.86
RFX5MA0510.2chr14:24549049-24549065GGTTACCATGGAAACT+6.75
RFX5MA0510.2chr14:24549049-24549065GGTTACCATGGAAACT-6.83
ZNF263MA0528.1chr14:24548845-24548866TGGGGAGGGGGTGGAGAGAGG+6.14
ZNF263MA0528.1chr14:24549254-24549275CTCTCTCCCTCTCTCTCCCTC-6.27
ZNF263MA0528.1chr14:24548794-24548815AGAGGAGGGGAAAGAGGGAGC+6.61
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr142454741724547612
Number: 1             
IDChromosomeStartEnd
GH14I024079chr142454902124549170
Enhancer Sequence
CATCATGCCT CAGATGCCCA CTGGGCAGCC TGCAGCACCC CCACACACAC CATAAGAAAT 60
GAGGACCAGC ACCTTTCAAA ATCTGAGACA GAGCTCCCCA GGCAGGCTGC TGTCTCTGCA 120
GTCTTACCCC AGCTATGTGC CAGTGGGATC TGAGGAGCCC CCTCCCTCAC CTCCCAACCC 180
CAGGGGGTCT AGGCACCATG GAGAATAATT ACAGGAGATA GGAGGATAAT TACGGGCTGT 240
CAGGAGGGCA GGCTGAAGCT TTCTTATAGC TGTCTCCAGA GAGGCCCTGC TGAGTCCCCC 300
AGGAGCTGAA CCCCAGCCCC CACACAGCTG TGGGGCGGGC CAAGAGCAGG TGCTGGGGGA 360
TACTGAAGGA GGGCAGCAGG TCTGCTAGTG AATTGGGAAC ATAGTGGAGC ATCTAAGGCC 420
TATACAGTCT GGTTTCCCGG GTGTGTCAAT GTGTGTGTCT GTTCATGGCC TTAATGGGTC 480
ACACTCATGG ACTCAGGGAT GTGCAGTGCA TGAACACACA GATTCACACA CTTAACAATC 540
ACATCAGCAA CAACAGCAAA TATCATTACG TAGCATGTGT CAACTTTATG CTAAGTGCTT 600
ATTTAAATGC ATTTATTCTC AGTAGGTGGT TACCATTATT TTCACCATTT TTCTGACAAT 660
CAAGTGAGGC TTGATTTTAA CCCACCCATG GTCAAAAAAC TGGTAGAACT GCAACTTGAA 720
ACAGGGTCTC ACTCTGCCAC CCAGGCTGGA ATGCAGTGGC ACGATTATGG CTCACTGCAT 780
CCCCGAACTC CTGGGCTCAA GTTATCCTTC CACCTTAGCC TCCTGGGTAG GTGGGACTCC 840
AGGTGCATGC CATTACATCT GAATTTATTT TATTTTATTT TTTTGTAGTG ACAGGGTTCT 900
CGCTATGTTG CCCAGGCTGG TCTCAAACTT CCTCCTTGGC CTCCCAAAGT GTTGGGATTA 960
CAGGCAGGAA CCACTGCGCC CCACCTAAAG CACTACTCTT AATCACCACA GTGTGCAACT 1020
TTGTTTTTTT AAGTATACTC AGGTAACCCA GGAGTATCAT TTTGAGACCC AGGTATGGTA 1080
CTGTATATGT GGCCTAGTTG TGTGCTCAGG TGTCTATGGA TGGTTCTGTC TGTCTTTGTG 1140
TGCCATGCAG GTGAGAAAAG TGAACAAGAA AAGTAGTGGG TCTGAATTAC AGCTCCAGGG 1200
CAGGCAAGGA TAGACACAGG TGAAATTTAG AGTGAGAGAA AAAGAGCTGG GCTCCCGGAA 1260
GGACCCTCCC TGCCCCATCC TCTCCCTTCA ACAATGAGTG TGGAAGGGGA TGAAGAAAGA 1320
GAAGCTAAAG GTTCTGTGAG CCCCTCAGAG AGAGAATCCA GAGCCAGAGA GGATGGCCAG 1380
TGGCCAATGG TGGGGAAGGG AGAGGAGACG AGAGAAATTC TGAGAGCGAT GGAGGAGAGG 1440
ACTCCCATTG CAGGCTCCTA AGCGGAGGAG GGATGAGCTG GGATAGAGGA GGGGAAAGAG 1500
GGAGCAAGAA CTGTGATGGG AAGAGAAGAG ACAGCTGGGG AGGGGGTGGA GAGAGGGGGT 1560
AGAAAGGAAG AGGGACATAT GGGAGCCTCT TCCCCCATGC CCGAAAGCTT CTCCCATTTA 1620
TTATGTCCGG TAGAGGACAG ATGACAGTAA CTCGTGAGGC GGCTGCTCCC AGCACAACGC 1680
CTGTGCTCTG CCCAGAGGCC CCATCTGCCC TCCCCTTAGC CTGCTGAACT GGAGGACTGG 1740
GTTACCATGG AAACTGTGAG ACCTGGATAG CCACTGACAG GCCGAGCTGG GCCACTGAGG 1800
CTTCTGAGTT TGGTGGTGGT GGTGGTGAGA GGGGGAGGAT CCATCTGTTC CAATGCCTGC 1860
CCCTCCACCC CATTTCCATT GGCTCTCCAT AACAGATGTG CCACCCAGCT CCAGGTGGGG 1920
ACTTCCCTTT TTCTTGCTCT CTCTCTCTCT CCCTCTCTCT CCCTCTCCCA CACACAGACA 1980
CACAAACAGT AGCCTGAAGC 2000