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

TagContent
EnhancerAtlas ID
HS146-06490 
Organism
Homo sapiens 
Tissue/cell
NHDF 
Coordinate
chr17:43247450-43250750 
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
CATTTGCCCC AGAGAGGTCT GAGTGGGGTC CCAGTCCCTG CTGCCCCAAG CCTGGCAGGA 60
CAGCAGACCT CTGGATGGGG ACCTCCCAAG GTCTCCGGGA TACCTGAATC CTGCTCTGTG 120
GGTGTTGGAG CAATCAGACT GCACAGAAGG TTTTCTAGGT GGGAGGGAGT TCAGTCAGGA 180
GCCCCCAGTT TCGGCCAGAA ACTGACGCTC AAGATACCAG ATCGCTGTGA GGAGTTGTGA 240
GCTTTCCCTG GAGGAGAGAA CGGGGGTTTT CGGAGAAGAC CCAGGCCCAG GGGTTCCTTC 300
AGAGTTTGCT CCTGAGCTCC CTGTATTCTC CCCACAGTTT AAAGGCTGGA CTAGACGGGT 360
TCTGGGTGCC TTGTGCCTCC TTGTTCTTGA CAGCCCCCAA CCCTGACCCC TCTCTGCAGG 420
GGGTTGGGCC TGAGGTTAGT CATCATGTGT TTGTGTTTGT CCCTTACCTC CCAAGGGTAA 480
TAAGGGAGGC GCTCTCCTGA TGGAAAATAA AGTCAAGAGA CAGAGGGGGA CAGCACATGG 540
ATCGCCAGCA GAGCAGAGCA GCCTGGCTCT CCTGGTGCCT GCCATGTGTC TGTGCGTCCT 600
GCTCCTCTCA GCCTCATCAT GTGGGTGTGA ATTCTCTGAA GTGTGTGAGG CCCTCGCCTG 660
TCTGCATCAG AGAGAGCTGG GTCAGCCTGG GTAACGCAGA TACCACCAGC CAGCGTCAGG 720
CTCTGAGACA AGCTCACCCA CCCCCTCGCA CTCAGACCCA CCCTTCCCCA GACACCCTGT 780
CTCTTCCATC CCCTCCTGGT GCCCTTGCAG ACTGGTGTTG GGTGTCAGGC AGCAATGAAC 840
ATGGACAACT AATGGTGGCG GAGGAAATTA GTCAACTCAC CAGTGAGCCA GTGCTGGCTG 900
TGCCACCAGG CAAGGGGAGG GGCAGAGGCC TGGCTGCCCA GTCTGGCTTC TCTTCCAGGC 960
CGTCATCTTG ACAGGCCACA CTGGGCAAGA TGAGGCTTGG CCCAGGAGCT GCTGGGGATG 1020
GAAATGTTGA TGAAATCTTG TGTGTTGCCA GGACAACTTT CATTTCTATC CTGCCACACC 1080
CAGGCCTGGC CAGAGCCTCC TACAATGAAA CACAGAACAG ATTCTAGGAA CGCATGGGTT 1140
TCAAGAGAAA GCAAAATCTC ATCCTGGGAG ACCTGCCCCT GGAACCCTGG GTCCTCAGAC 1200
AGCTCAGTCA GGAAGGGCAG CAGGAATGAT CATCGCCACT TTGCAGACGG GAAACCGGAG 1260
GCTTAGCGAG GAAGTGGCTT TTTGGATTCC AGGAGAGCCT CTGGAGGCCT GCCTGCCCCT 1320
GTGGGGTGCT GTGGGGTGCT AGCCTGGGAC CCAGAGGCCC CTTGGCATTT GCTGGCAGCC 1380
TCCCAGCTGC ATTCCTCAGC ATGGAGCCCG AGGGAGAGAG GAGGCCTGGG ACAAAGGTGG 1440
ACAAAGGTTG TTTACCCGGA GGTGCCTCTG TGTGTGTGTG TCTAGGAGGT GAGAGAAGAT 1500
TCCAGAGGGC TGCTGGAGTG TCGGGGGAGG GGTGTGGGTG AGGGTGCTGG GTGCTCATTG 1560
TGGGCTGGTT ATGCCAGGGA GGGGCAGGTG AAGAGTTTGG CCTTTCTTGG CCCAGAAGCT 1620
GAGGAGCCTG GAGGCAGGGA AGCTGCCAGC TGCTCCTCCA ACATCCCCCT TACACGTAAA 1680
AGGCTGAAGG GCGCAAATAG GGCAGCACCT CGGTGGGTTA ATTCCCGCAC CCCCACCTCA 1740
CCCCGCTGGA GGGCGGGTGG GGCAAGAAGA GAACAAAGGA GAGGATGCTA GCCGGGAGTG 1800
TGGGAGGGCC TGAACCCAAA TGGGAGGGGT CCGTGAAAAG GGTCCCTGTC TGCCCCTCCC 1860
CCTGTCTGGC TCCCTGATTC CTGGGTAAGG GGTGTGCAGG GAGGAGATCG TCCTGGGGCC 1920
AGAGCTGGGG CTTAGCACTG GAGAGAACCG GCTCAGCTGT GGGTGGGAGC CAGGCCTGGG 1980
TCCCTCGGTG CCCCGCCCCC TTCGCTGCTT CCAGTTGTTC CCACACCTGC TGCTTGGTCT 2040
TGAAGCCTGG GCCTCCACTC CGCCTACTGC AATGGTGGAA GCTCCAGTTT ACAAGACACC 2100
CCCACCCCCA CATCACACGC CCTAGCTGGG GAAGTTGGGC TTGGACACAG CCTCCCTGGG 2160
CCTTTCCACA GCTGCCCTCA CGCCCTGTGC TTTCTGGGAC CCTCTTGGTC AACTGGGCCG 2220
GGGAAGGGAA GCGCAGAGAA CATATGTTTC ATGGGAGTGA CTGTTGAAGC CTCCCACCAC 2280
CCCTGCCCAG CCTGTCTTAG GATCCCTCTT TCTTCCCCGG CAGGAACTGC CCGACCCCAG 2340
GTGGAAACTC CTGTGCCCAG TGGACAGACC CTGCCTGCAA TAGGGTCAGA GTATGAGGGA 2400
GAGGGGTAGG CAGAGATTGG TGGGCTGGGG CAGGAAGAAG CTGCCAGGGA GTGGGGGGAG 2460
GGGGTCCAAA GGGAAGTAAC GGTATTGGGG GGAAAGGTGG CCAGGTCCCA TTGCCCTTGT 2520
TGGGAACAGG CAAGTGTGGC ACTGGCCCTT TAAGTGGGGG TGCCAGTCAG TGCCCTCCCC 2580
CAACCAACCC AATTCATGGG CACACTGAGC ATGTGCAGGG GCTGTGCATG TGGGGAGGGG 2640
AGGAGAGGGG AGGGGAGAGG GGGGCATACA TTCCGGAGGG AGCTTCTCAT CCCCCTACTT 2700
CCGGTAGCTG CCCCCACTCT CCTTCCTGGG TCTGACAAAG GAGCCCATGG TGCTCACCCA 2760
ATCCCTTCCC CCACCCCAGG CCCCAGGGGG TGCTGCCCTC TGCAAGTGCT GAAGCTGCCA 2820
TGGGTGCTGG GCAGGCCCTC TCTGCCCTGG GGAGTCTCCT GGCCGCCTGG AGGTGGCACA 2880
CATGCAGCCC AGTGCCGGCC TCACTTCCCT GGTGTGGGCG GCGGCGAATC TTCCTGCTGC 2940
CTACGTGTTC CATTTCATTC CATTGGTGCC AGGGTTTTTA AAAGAACCAT CCACCTGTGA 3000
TGCCACTTTG AAAGTGAAAC AGCTCAAAGG ATGCAGGCCC TACCCCCTAA CCAGGACCTT 3060
CCAGTCAGAG AGGAAGCAAA CAGCCCAGAG GCTGCAAGGG CCTTCCTTGA ATCCCGCTCC 3120
TTCTGCTTCT CCCCTGCTGG CCAAGGGATC AAAGTCAGCT TCCTCCAGAC TACCTTCACC 3180
TGCAGCCTGG GACCTTCCCT CAAACCTTTC CACCACCTAA ACCTTACCTG TTTCTGCCAA 3240
GTCTTCCCCT CTCCCAGCCC TCAGCCCCTC CTGTTACCAC CCCTACCTCT TTAGCACTTG 3300