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

TagContent
EnhancerAtlas ID
HS076-28456 
Organism
Homo sapiens 
Tissue/cell
H1 
Coordinate
chr19:14495600-14497880 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr19:14495785-14495806CTTTTCTTTCTTTTTTTTTTT+6.41
NFKB1MA0105.4chr19:14496355-14496368GGGGGAACCCCCT+6.04
NFKB1MA0105.4chr19:14496355-14496368GGGGGAACCCCCT-6
ZfxMA0146.2chr19:14496826-14496840CCCGCCTCGGCCTC+6.01
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_09406chr19:14490810-14496956CD14
SE_10220chr19:14494179-14495842CD19_Primary
SE_10950chr19:14488467-14497186CD20
SE_11837chr19:14489865-14496949CD3
SE_12943chr19:14494080-14495836CD34_Primary_RO01480
SE_12943chr19:14495914-14496567CD34_Primary_RO01480
SE_13526chr19:14494118-14496781CD34_Primary_RO01536
SE_14178chr19:14494012-14496897CD34_Primary_RO01549
SE_14416chr19:14489601-14496960CD4_Memory_Primary_7pool
SE_16317chr19:14490754-14496927CD4_Naive_Primary_8pool
SE_16867chr19:14490708-14496826CD4p_CD225int_CD127p_Tmem
SE_17824chr19:14489766-14497244CD4p_CD25-_CD45ROp_Memory
SE_18377chr19:14490149-14497123CD4p_CD25-_Il17-_PMAstim_Th
SE_19159chr19:14490345-14496926CD4p_CD25-_Il17p_PMAstim_Th17
SE_19988chr19:14489520-14497100CD56
SE_20741chr19:14490667-14497165CD8_Memory_7pool
SE_21447chr19:14490705-14496703CD8_Naive_7pool
SE_21965chr19:14490812-14496814CD8_Naive_8pool
SE_22295chr19:14489493-14497075CD8_primiary
SE_23938chr19:14496249-14496614Colon_Crypt_2
SE_30750chr19:14494199-14495880Fetal_Muscle
SE_40289chr19:14494020-14495916K562
SE_40289chr19:14495984-14496814K562
SE_42847chr19:14494177-14495905Lung
SE_50325chr19:14494255-14495988Sigmoid_Colon
SE_52719chr19:14494187-14495865Small_Intestine
SE_53468chr19:14491024-14495912Spleen
SE_53468chr19:14495994-14496960Spleen
SE_62560chr19:14458771-14497116Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr191449704114497178
Number: 1             
IDChromosomeStartEnd
GH19I014386chr191449773214498426
Enhancer Sequence
CATGTAATTT CTGTCTCTCT GTCTGTCTCT ATCTCTCCGT GTCTCTGTCT CCTCTGTCTT 60
ATATTTCTCT AGCTGTCTTC TTTCTCCTCT CTGTCTCCCT CTCTCTCTCC AGCTTGTCTC 120
CTTTCTCCTC TCTGTCTCCG TCTCTGTCCC TCTATCTCTC TGTCTCTCTC TCTCTTTGTT 180
CTTTTCTTTT CTTTCTTTTT TTTTTTTTTG AGACTCTTGC TCTTTTTTTT TTTTTTTTTT 240
TTTTGAGAGT CTTGCTCTGT TGCCCAGGCT GGCGTGCAGT GGCGGGATCT CAGCTCACTG 300
CAACCTCTGC CTTCTGTGTT CAAGCGATTC TCCTGCCTCC ACCTCCCAAA TAGCTGGGAT 360
TACAGGCGTG TGCCACCATG CCCGGCTAAT TTTTTGTATT TTTAGTAGAG ATGGGGTTTC 420
ACTATGTTGG CCAGGCTGGT CTCACACTCC TGGCCTCAGG TGATCCATCT GCCTCGGCCT 480
CCCAAAGTGC TGGGATTACA GGCGTGAACC ACCAAGCACA GCCCCCCACC TTCTGTCTCT 540
CTGTCTCTTT GTGTCTCTGT CTCTCTTTCT GTGTCTCTCT TTCTTTCTGA CTCTTTCTCT 600
CTCTCTGTCT GTCTCTCTCT CTCTCTAATC TCTATTTTCT CTCCACCCCT GCTTCTTTGT 660
CTCTATCTCT CTGGTGAACA GCAAGGAGAT CCCTAGGTCC CCATCTCTGA ATCCCCTGGT 720
GACCTGAGGA GGGTCCCCCA GAACATGCCT TGGGAGGGGG AACCCCCTGA GTGCTGGGAA 780
CCGCCACTCC ACGTGCACCC CAACAGGCGG CTACAGCGTC TTCCTGTGGG AGGGGGGCCC 840
GGGGGTGAAA TATCACCACT GGGTTCCAGG ACAGACCGCC AGGGCCAGTG GCAGTTGTGG 900
GTGTGGTGTG TGTGCACCTG TGTCCCTGAG GAAGCGTGGA GGTCCAGGGC ATCTCAGAGC 960
CTGGGTGATC CAACACCGTC ATTTTTTTTT TTTTTTTTCT GAGACGGAGT CTTGCTCTGT 1020
CACTCAGGCT GGAGTGCAGT GGCGTGATCT TGGCTTGCTG CAACTCTGCC TCCTTAGTTC 1080
AAGCGATTCT CAAGCCTCAG TCTCCCAAGT AGCTGGGATA ACAGGCACCC ACCACCACGC 1140
CCAGCTAATT TTTTGTATTT TCAGTAGAGA GGGGGTTTCA CCATATTAGG CAGGCTGGTC 1200
TCGAACTCCC GATCTCAAGT GATCCACCCG CCTCGGCCTC CCAAAGTGCT GGGATTACAG 1260
GCATGAGCCA CTGTGCCTGA CCACGCCTTC ATTTTTACCT AAAGAAATGA AGATGGCAGG 1320
CAGGGCCTGG CGGCTTGTGC CAGCACTTTG GGAGGCCAAG GCAGGTGGAT CACGAGGTCA 1380
GGAGATCGAA ACCATCCTGG CTAACATGGT GAAACCCCTT CTCTACTAAA AATATAAAAA 1440
GTTAGCCAGG CGTGGTGGTG GGCGCCAGTA GTTCCAGCTA CTCTGGAGGC TGAGGCAGGA 1500
GAATGGCGTG AACCCGGGAG GTGGAGCTTG CAGTGAGCAG AGATCACACC ACTGCACTTC 1560
ATCCTGGGCA ACAGAGCAAG ACTCCATCTC AAAAAAAAAA AAAAAAAAAA AAAAAAGAGA 1620
GGCCGGGCGC GGTGGCTCAC GCCTGTAATT CCAGCACTTT GGGAGGCTGA GGCGGGCGGA 1680
TCATGAGGTC AGGAGATCAA GACTACCATC CTGGCTAACA TGGTGAAACC TTGTCTCTAC 1740
TAAAAATACA AAAAAATAAG CTGGGCGTGG TGGCGGGAGC CTGTGGTCCC AGCTACTCGA 1800
GAGGCTGAGA CAGGAGAATG GTGTGAACCC GGGAGGCGGA GCTTGCAGTG AGCCAAGTTT 1860
GCACCACTGC ACTCCAGCCT GGGCGACAGA GCAAGACTCC GTCTCAAAAA AAAAAAAAAA 1920
AAAAAAGAGA AATGAAGATG GCAGGCTGGG CACGGTGGCT CACGCCTGTA ATCCCAGCAC 1980
TTTTGGAGGC CAAGGCGGGA GGATCACTTG AGGCCGGGAG TTCAAGACCA GCCTGGCCAA 2040
CATGGTGAAA CCCCGTCTCT ACAAAAATAC AAAAAAATCA GCCGGGCTTG GTGGCGGGTG 2100
CCTGTAATCC CAGATACTCT GGAGACTGAG GCAGAGGAAT TGCTTGAACC CGGGAGGTGG 2160
AGGTTGCAGT GAGCCAGGAT CGTGCCATCG CACTCCAGCC TGGGCGACAG AGAGAGACTC 2220
TGTCTCAGAA AAAAAATAAA ATAAATAAAT AAATAAAAGA AGAAGAAATG AAGATGGCAG 2280