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

TagContent
EnhancerAtlas ID
HS098-24148 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr17:43247540-43250770 
SNPs
Number: 3             
IDChromosomePositionGenome Version
rs4792819chr1743247957hg19
rs4792867chr1743249444hg19
rs66827053chr1743250653hg19
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Atoh1MA0461.2chr17:43249688-43249698AACATATGTT+6.02
Atoh1MA0461.2chr17:43249688-43249698AACATATGTT-6.02
KLF16MA0741.1chr17:43249439-43249450GCCCCGCCCCC+6.02
KLF5MA0599.1chr17:43249439-43249449GCCCCGCCCC+6.02
RREB1MA0073.1chr17:43250026-43250046CCCCCAACCAACCCAATTCA+6.61
ZNF263MA0528.1chr17:43250080-43250101TGGGGAGGGGAGGAGAGGGGA+6.27
ZNF263MA0528.1chr17:43250085-43250106AGGGGAGGAGAGGGGAGGGGA+7.13
ZNF263MA0528.1chr17:43250088-43250109GGAGGAGAGGGGAGGGGAGAG+7.79
Number of super-enhancer constituents: 21             
IDCoordinateTissue/cell
SE_04340chr17:43247900-43250852Brain_Anterior_Caudate
SE_05493chr17:43247643-43251138Brain_Cingulate_Gyrus
SE_08396chr17:43247530-43251110Brain_Inferior_Temporal_Lobe
SE_11664chr17:43249023-43251261CD20
SE_14897chr17:43249828-43250904CD4_Memory_Primary_7pool
SE_17616chr17:43248328-43250887CD4p_CD25-_CD45RAp_Naive
SE_26109chr17:43247379-43251134Duodenum_Smooth_Muscle
SE_30505chr17:43246948-43250903Fetal_Muscle
SE_34119chr17:43247378-43250989HCC1954
SE_34723chr17:43246812-43254725HeLa
SE_35335chr17:43247011-43251161HepG2
SE_37184chr17:43246945-43251043HSMMtube
SE_41920chr17:43247951-43250628LNCaP
SE_46560chr17:43247407-43250979Osteoblasts
SE_52300chr17:43247539-43250784Skeletal_Muscle_Myoblast
SE_53522chr17:43247744-43250887Spleen
SE_54753chr17:43246796-43250862Stomach_Smooth_Muscle
SE_57115chr17:43247779-43250829VACO_400
SE_58198chr17:43247689-43250776VACO_9m
SE_66823chr17:43248412-43250792Jurkat
SE_68795chr17:43247672-43251035H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr174324998943250354
Number: 1             
IDChromosomeStartEnd
GH17I045168chr174324620943251994
Enhancer Sequence
GTCTCCGGGA TACCTGAATC CTGCTCTGTG GGTGTTGGAG CAATCAGACT GCACAGAAGG 60
TTTTCTAGGT GGGAGGGAGT TCAGTCAGGA GCCCCCAGTT TCGGCCAGAA ACTGACGCTC 120
AAGATACCAG ATCGCTGTGA GGAGTTGTGA GCTTTCCCTG GAGGAGAGAA CGGGGGTTTT 180
CGGAGAAGAC CCAGGCCCAG GGGTTCCTTC AGAGTTTGCT CCTGAGCTCC CTGTATTCTC 240
CCCACAGTTT AAAGGCTGGA CTAGACGGGT TCTGGGTGCC TTGTGCCTCC TTGTTCTTGA 300
CAGCCCCCAA CCCTGACCCC TCTCTGCAGG GGGTTGGGCC TGAGGTTAGT CATCATGTGT 360
TTGTGTTTGT CCCTTACCTC CCAAGGGTAA TAAGGGAGGC GCTCTCCTGA TGGAAAATAA 420
AGTCAAGAGA CAGAGGGGGA CAGCACATGG ATCGCCAGCA GAGCAGAGCA GCCTGGCTCT 480
CCTGGTGCCT GCCATGTGTC TGTGCGTCCT GCTCCTCTCA GCCTCATCAT GTGGGTGTGA 540
ATTCTCTGAA GTGTGTGAGG CCCTCGCCTG TCTGCATCAG AGAGAGCTGG GTCAGCCTGG 600
GTAACGCAGA TACCACCAGC CAGCGTCAGG CTCTGAGACA AGCTCACCCA CCCCCTCGCA 660
CTCAGACCCA CCCTTCCCCA GACACCCTGT CTCTTCCATC CCCTCCTGGT GCCCTTGCAG 720
ACTGGTGTTG GGTGTCAGGC AGCAATGAAC ATGGACAACT AATGGTGGCG GAGGAAATTA 780
GTCAACTCAC CAGTGAGCCA GTGCTGGCTG TGCCACCAGG CAAGGGGAGG GGCAGAGGCC 840
TGGCTGCCCA GTCTGGCTTC TCTTCCAGGC CGTCATCTTG ACAGGCCACA CTGGGCAAGA 900
TGAGGCTTGG CCCAGGAGCT GCTGGGGATG GAAATGTTGA TGAAATCTTG TGTGTTGCCA 960
GGACAACTTT CATTTCTATC CTGCCACACC CAGGCCTGGC CAGAGCCTCC TACAATGAAA 1020
CACAGAACAG ATTCTAGGAA CGCATGGGTT TCAAGAGAAA GCAAAATCTC ATCCTGGGAG 1080
ACCTGCCCCT GGAACCCTGG GTCCTCAGAC AGCTCAGTCA GGAAGGGCAG CAGGAATGAT 1140
CATCGCCACT TTGCAGACGG GAAACCGGAG GCTTAGCGAG GAAGTGGCTT TTTGGATTCC 1200
AGGAGAGCCT CTGGAGGCCT GCCTGCCCCT GTGGGGTGCT GTGGGGTGCT AGCCTGGGAC 1260
CCAGAGGCCC CTTGGCATTT GCTGGCAGCC TCCCAGCTGC ATTCCTCAGC ATGGAGCCCG 1320
AGGGAGAGAG GAGGCCTGGG ACAAAGGTGG ACAAAGGTTG TTTACCCGGA GGTGCCTCTG 1380
TGTGTGTGTG TCTAGGAGGT GAGAGAAGAT TCCAGAGGGC TGCTGGAGTG TCGGGGGAGG 1440
GGTGTGGGTG AGGGTGCTGG GTGCTCATTG TGGGCTGGTT ATGCCAGGGA GGGGCAGGTG 1500
AAGAGTTTGG CCTTTCTTGG CCCAGAAGCT GAGGAGCCTG GAGGCAGGGA AGCTGCCAGC 1560
TGCTCCTCCA ACATCCCCCT TACACGTAAA AGGCTGAAGG GCGCAAATAG GGCAGCACCT 1620
CGGTGGGTTA ATTCCCGCAC CCCCACCTCA CCCCGCTGGA GGGCGGGTGG GGCAAGAAGA 1680
GAACAAAGGA GAGGATGCTA GCCGGGAGTG TGGGAGGGCC TGAACCCAAA TGGGAGGGGT 1740
CCGTGAAAAG GGTCCCTGTC TGCCCCTCCC CCTGTCTGGC TCCCTGATTC CTGGGTAAGG 1800
GGTGTGCAGG GAGGAGATCG TCCTGGGGCC AGAGCTGGGG CTTAGCACTG GAGAGAACCG 1860
GCTCAGCTGT GGGTGGGAGC CAGGCCTGGG TCCCTCGGTG CCCCGCCCCC TTCGCTGCTT 1920
CCAGTTGTTC CCACACCTGC TGCTTGGTCT TGAAGCCTGG GCCTCCACTC CGCCTACTGC 1980
AATGGTGGAA GCTCCAGTTT ACAAGACACC CCCACCCCCA CATCACACGC CCTAGCTGGG 2040
GAAGTTGGGC TTGGACACAG CCTCCCTGGG CCTTTCCACA GCTGCCCTCA CGCCCTGTGC 2100
TTTCTGGGAC CCTCTTGGTC AACTGGGCCG GGGAAGGGAA GCGCAGAGAA CATATGTTTC 2160
ATGGGAGTGA CTGTTGAAGC CTCCCACCAC CCCTGCCCAG CCTGTCTTAG GATCCCTCTT 2220
TCTTCCCCGG CAGGAACTGC CCGACCCCAG GTGGAAACTC CTGTGCCCAG TGGACAGACC 2280
CTGCCTGCAA TAGGGTCAGA GTATGAGGGA GAGGGGTAGG CAGAGATTGG TGGGCTGGGG 2340
CAGGAAGAAG CTGCCAGGGA GTGGGGGGAG GGGGTCCAAA GGGAAGTAAC GGTATTGGGG 2400
GGAAAGGTGG CCAGGTCCCA TTGCCCTTGT TGGGAACAGG CAAGTGTGGC ACTGGCCCTT 2460
TAAGTGGGGG TGCCAGTCAG TGCCCTCCCC CAACCAACCC AATTCATGGG CACACTGAGC 2520
ATGTGCAGGG GCTGTGCATG TGGGGAGGGG AGGAGAGGGG AGGGGAGAGG GGGGCATACA 2580
TTCCGGAGGG AGCTTCTCAT CCCCCTACTT CCGGTAGCTG CCCCCACTCT CCTTCCTGGG 2640
TCTGACAAAG GAGCCCATGG TGCTCACCCA ATCCCTTCCC CCACCCCAGG CCCCAGGGGG 2700
TGCTGCCCTC TGCAAGTGCT GAAGCTGCCA TGGGTGCTGG GCAGGCCCTC TCTGCCCTGG 2760
GGAGTCTCCT GGCCGCCTGG AGGTGGCACA CATGCAGCCC AGTGCCGGCC TCACTTCCCT 2820
GGTGTGGGCG GCGGCGAATC TTCCTGCTGC CTACGTGTTC CATTTCATTC CATTGGTGCC 2880
AGGGTTTTTA AAAGAACCAT CCACCTGTGA TGCCACTTTG AAAGTGAAAC AGCTCAAAGG 2940
ATGCAGGCCC TACCCCCTAA CCAGGACCTT CCAGTCAGAG AGGAAGCAAA CAGCCCAGAG 3000
GCTGCAAGGG CCTTCCTTGA ATCCCGCTCC TTCTGCTTCT CCCCTGCTGG CCAAGGGATC 3060
AAAGTCAGCT TCCTCCAGAC TACCTTCACC TGCAGCCTGG GACCTTCCCT CAAACCTTTC 3120
CACCACCTAA ACCTTACCTG TTTCTGCCAA GTCTTCCCCT CTCCCAGCCC TCAGCCCCTC 3180
CTGTTACCAC CCCTACCTCT TTAGCACTTG TCCACTCTTA GCTACTGGTA 3230