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

TagContent
EnhancerAtlas ID
HS076-24960 
Organism
Homo sapiens 
Tissue/cell
H1 
Coordinate
chr17:43247940-43250740 
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
GCTCTCCTGA TGGAAAATAA AGTCAAGAGA CAGAGGGGGA CAGCACATGG ATCGCCAGCA 60
GAGCAGAGCA GCCTGGCTCT CCTGGTGCCT GCCATGTGTC TGTGCGTCCT GCTCCTCTCA 120
GCCTCATCAT GTGGGTGTGA ATTCTCTGAA GTGTGTGAGG CCCTCGCCTG TCTGCATCAG 180
AGAGAGCTGG GTCAGCCTGG GTAACGCAGA TACCACCAGC CAGCGTCAGG CTCTGAGACA 240
AGCTCACCCA CCCCCTCGCA CTCAGACCCA CCCTTCCCCA GACACCCTGT CTCTTCCATC 300
CCCTCCTGGT GCCCTTGCAG ACTGGTGTTG GGTGTCAGGC AGCAATGAAC ATGGACAACT 360
AATGGTGGCG GAGGAAATTA GTCAACTCAC CAGTGAGCCA GTGCTGGCTG TGCCACCAGG 420
CAAGGGGAGG GGCAGAGGCC TGGCTGCCCA GTCTGGCTTC TCTTCCAGGC CGTCATCTTG 480
ACAGGCCACA CTGGGCAAGA TGAGGCTTGG CCCAGGAGCT GCTGGGGATG GAAATGTTGA 540
TGAAATCTTG TGTGTTGCCA GGACAACTTT CATTTCTATC CTGCCACACC CAGGCCTGGC 600
CAGAGCCTCC TACAATGAAA CACAGAACAG ATTCTAGGAA CGCATGGGTT TCAAGAGAAA 660
GCAAAATCTC ATCCTGGGAG ACCTGCCCCT GGAACCCTGG GTCCTCAGAC AGCTCAGTCA 720
GGAAGGGCAG CAGGAATGAT CATCGCCACT TTGCAGACGG GAAACCGGAG GCTTAGCGAG 780
GAAGTGGCTT TTTGGATTCC AGGAGAGCCT CTGGAGGCCT GCCTGCCCCT GTGGGGTGCT 840
GTGGGGTGCT AGCCTGGGAC CCAGAGGCCC CTTGGCATTT GCTGGCAGCC TCCCAGCTGC 900
ATTCCTCAGC ATGGAGCCCG AGGGAGAGAG GAGGCCTGGG ACAAAGGTGG ACAAAGGTTG 960
TTTACCCGGA GGTGCCTCTG TGTGTGTGTG TCTAGGAGGT GAGAGAAGAT TCCAGAGGGC 1020
TGCTGGAGTG TCGGGGGAGG GGTGTGGGTG AGGGTGCTGG GTGCTCATTG TGGGCTGGTT 1080
ATGCCAGGGA GGGGCAGGTG AAGAGTTTGG CCTTTCTTGG CCCAGAAGCT GAGGAGCCTG 1140
GAGGCAGGGA AGCTGCCAGC TGCTCCTCCA ACATCCCCCT TACACGTAAA AGGCTGAAGG 1200
GCGCAAATAG GGCAGCACCT CGGTGGGTTA ATTCCCGCAC CCCCACCTCA CCCCGCTGGA 1260
GGGCGGGTGG GGCAAGAAGA GAACAAAGGA GAGGATGCTA GCCGGGAGTG TGGGAGGGCC 1320
TGAACCCAAA TGGGAGGGGT CCGTGAAAAG GGTCCCTGTC TGCCCCTCCC CCTGTCTGGC 1380
TCCCTGATTC CTGGGTAAGG GGTGTGCAGG GAGGAGATCG TCCTGGGGCC AGAGCTGGGG 1440
CTTAGCACTG GAGAGAACCG GCTCAGCTGT GGGTGGGAGC CAGGCCTGGG TCCCTCGGTG 1500
CCCCGCCCCC TTCGCTGCTT CCAGTTGTTC CCACACCTGC TGCTTGGTCT TGAAGCCTGG 1560
GCCTCCACTC CGCCTACTGC AATGGTGGAA GCTCCAGTTT ACAAGACACC CCCACCCCCA 1620
CATCACACGC CCTAGCTGGG GAAGTTGGGC TTGGACACAG CCTCCCTGGG CCTTTCCACA 1680
GCTGCCCTCA CGCCCTGTGC TTTCTGGGAC CCTCTTGGTC AACTGGGCCG GGGAAGGGAA 1740
GCGCAGAGAA CATATGTTTC ATGGGAGTGA CTGTTGAAGC CTCCCACCAC CCCTGCCCAG 1800
CCTGTCTTAG GATCCCTCTT TCTTCCCCGG CAGGAACTGC CCGACCCCAG GTGGAAACTC 1860
CTGTGCCCAG TGGACAGACC CTGCCTGCAA TAGGGTCAGA GTATGAGGGA GAGGGGTAGG 1920
CAGAGATTGG TGGGCTGGGG CAGGAAGAAG CTGCCAGGGA GTGGGGGGAG GGGGTCCAAA 1980
GGGAAGTAAC GGTATTGGGG GGAAAGGTGG CCAGGTCCCA TTGCCCTTGT TGGGAACAGG 2040
CAAGTGTGGC ACTGGCCCTT TAAGTGGGGG TGCCAGTCAG TGCCCTCCCC CAACCAACCC 2100
AATTCATGGG CACACTGAGC ATGTGCAGGG GCTGTGCATG TGGGGAGGGG AGGAGAGGGG 2160
AGGGGAGAGG GGGGCATACA TTCCGGAGGG AGCTTCTCAT CCCCCTACTT CCGGTAGCTG 2220
CCCCCACTCT CCTTCCTGGG TCTGACAAAG GAGCCCATGG TGCTCACCCA ATCCCTTCCC 2280
CCACCCCAGG CCCCAGGGGG TGCTGCCCTC TGCAAGTGCT GAAGCTGCCA TGGGTGCTGG 2340
GCAGGCCCTC TCTGCCCTGG GGAGTCTCCT GGCCGCCTGG AGGTGGCACA CATGCAGCCC 2400
AGTGCCGGCC TCACTTCCCT GGTGTGGGCG GCGGCGAATC TTCCTGCTGC CTACGTGTTC 2460
CATTTCATTC CATTGGTGCC AGGGTTTTTA AAAGAACCAT CCACCTGTGA TGCCACTTTG 2520
AAAGTGAAAC AGCTCAAAGG ATGCAGGCCC TACCCCCTAA CCAGGACCTT CCAGTCAGAG 2580
AGGAAGCAAA CAGCCCAGAG GCTGCAAGGG CCTTCCTTGA ATCCCGCTCC TTCTGCTTCT 2640
CCCCTGCTGG CCAAGGGATC AAAGTCAGCT TCCTCCAGAC TACCTTCACC TGCAGCCTGG 2700
GACCTTCCCT CAAACCTTTC CACCACCTAA ACCTTACCTG TTTCTGCCAA GTCTTCCCCT 2760
CTCCCAGCCC TCAGCCCCTC CTGTTACCAC CCCTACCTCT 2800