EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS046-13501 
Organism
Homo sapiens 
Tissue/cell
Fetal_muscle_leg 
Coordinate
chr16:11690600-11692470 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs8049607chr1611691753hg19
TF binding sites/motifs
Number: 16             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr16:11691757-11691778TTTTGCTTTCTTTTTTCTTTG+6.08
ZNF263MA0528.1chr16:11690602-11690623GGAAGAGAAGAAGGGAGAGGA+6.03
ZNF263MA0528.1chr16:11690661-11690682GAGGAAAGAAGAGGGGGAGGA+6.23
ZNF263MA0528.1chr16:11690632-11690653GGGGGACAGGGGAGAGGGGGA+6.28
ZNF263MA0528.1chr16:11690682-11690703GGAGGAGGTGGTGGGGAGGAG+6.33
ZNF263MA0528.1chr16:11690626-11690647GGGGGAGGGGGACAGGGGAGA+6.69
ZNF263MA0528.1chr16:11690605-11690626AGAGAAGAAGGGAGAGGAGGA+6.6
ZNF263MA0528.1chr16:11690664-11690685GAAAGAAGAGGGGGAGGAGGA+6.92
ZNF263MA0528.1chr16:11690620-11690641GGAGGAGGGGGAGGGGGACAG+7.25
ZNF263MA0528.1chr16:11690614-11690635GGGAGAGGAGGAGGGGGAGGG+7.33
ZNF263MA0528.1chr16:11690673-11690694GGGGGAGGAGGAGGAGGTGGT+7.3
ZNF263MA0528.1chr16:11690667-11690688AGAAGAGGGGGAGGAGGAGGA+7.4
ZNF263MA0528.1chr16:11690679-11690700GGAGGAGGAGGTGGTGGGGAG+7.83
ZNF263MA0528.1chr16:11690608-11690629GAAGAAGGGAGAGGAGGAGGG+8.08
ZNF263MA0528.1chr16:11690676-11690697GGAGGAGGAGGAGGTGGTGGG+8.33
ZNF263MA0528.1chr16:11690617-11690638AGAGGAGGAGGGGGAGGGGGA+9.92
Number of super-enhancer constituents: 10             
IDCoordinateTissue/cell
SE_10082chr16:11689593-11693821CD14
SE_17577chr16:11690659-11691761CD4p_CD25-_CD45RAp_Naive
SE_23656chr16:11689754-11691932Colon_Crypt_1
SE_27070chr16:11690611-11691856Esophagus
SE_31920chr16:11690668-11691863Gastric
SE_42648chr16:11690481-11692793Lung
SE_50207chr16:11690423-11692737Sigmoid_Colon
SE_52871chr16:11690621-11691947Small_Intestine
SE_53430chr16:11688679-11693985Spleen
SE_61608chr16:11668804-11735966Toledo
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr161169100311692063
Number: 1             
IDChromosomeStartEnd
GH16I011595chr161168885811693256
Enhancer Sequence
GAGGAAGAGA AGAAGGGAGA GGAGGAGGGG GAGGGGGACA GGGGAGAGGG GGAAGGGACA 60
GGAGGAAAGA AGAGGGGGAG GAGGAGGAGG TGGTGGGGAG GAGGAAGACA GTGATGGGCA 120
CACAAGCTGA GTACCCACTG GGTGCCAGGC CCTGGAATGT AAAAGCACTT TTACATCCAC 180
CATCTCATTT TCTCCTTACA ACAATCCAGC TGTTTTACAG ATTAGGCAAC TGAAGCCCAG 240
ACAGGTAAAG TAACATGCCT CGAATCACAG AGCAAGAAGG TGACTACAGG TAAAATTTGC 300
ACCAGGTCTG GCTGATTCGT GAAGTTGTCA GGCAGCTTTC TCACCCTCTC AGGTGATGTG 360
TCCTAGGAAC CAGGCACCAT TTCAGGAGCT AGAACTGGGG TAACAAGATA GCGGTCCCAA 420
CTCCCCTGGA GTTTATATTC TGGTTAGGAG CAGGGGAGGA AAAATCCACA ATAAACAAGT 480
ACCCTGTGAC TTTGGGGTCA TCTACTGGCA CTTTCTCTTC CTTGTAGCCT CCAGGAAACA 540
CACGTCTTCA TAACACAGAA GAATTTCATT CTTTGAGCTC CATTCCACAA CCCACTGGGG 600
GTGTGGGGAG AGGCTGGGCA GTGGAGTGCG GGTGGAGCAT GAGTCATAGA ATTATAGTCG 660
CCTAACAAAC AGTCACAGTC ACATAGGCCA CCAGACTCCT CTCTCCCAGC AACCCTATAA 720
GGGAAATATT ATCATCTCCG CTTTACAGAC TTAGCAATAC AGGCCCAGAG AGGTCAGGCA 780
GGTTGTCAAA GGTCACACAG CCAGCACATG GCAGCAGTAG GATTTGAACC CAAGCTGTCT 840
GGCTCTACGT CCATGCTCAG CCCCCATGCT GTGGAGAGCT TAGAGCTTTC TAGATGGCCC 900
AGATCTGTGA CTTTCTGGCC ACAGAACCTA AGAACCTTCC CTTCCAAAAC AGTGTCCTAC 960
AGAGCCCAAC TCACAGAACA GAAACAAGCA GTTCTGTGTG AGGTGAGGCA AGTCCCTGCC 1020
CTCCGCAGTC TGAAGGAGAG CCCTCTGCCT GTTTTCCCCG CTCCAGCCCC GTCATTTTAT 1080
AGCTGAGGCC CAGAAAGGGG TTGAGGAGCT AAAGGCCCCA CAGCCAGGCT GGAAATGGGA 1140
CAAAACCCAG CATGCTTTTT TGCTTTCTTT TTTCTTTGTA GAGACAGGGT CTTGTGTAGT 1200
CACCCAGGCT GGAGTGCAGT GGCGCTATCA TAGCTCACTG CAGCCTCTAC CTCCTGAGCA 1260
CAGCAATTCT CCCGCCTCAG ACACCCGAGT AGCTGGGACT ACAGGCATGC GCCACCACGC 1320
CCGGGTAATT TTTTACTTTT TGTAGAGATG GGTTTCCCAG GCTAATCTTA AACTTAATCC 1380
TAGGCTCAAG TGATCCTCCT GCCTCAGCCT CCCAAGGTGC TGGAATTACA GGCATGAGCC 1440
TCTGTGCCCG GCCAAAAGCT CAGCACTCTT GGGTCTCCAT GCAAGTTTCT CTCCTCTCTT 1500
GGGGCACCCA CTGAGGCCCC ACTGTCTCTC CAGGGCCTGA GCCTTTTTTT TTTTTTTGCC 1560
CCAGACAACA ACAAGCCAAG ATGCCACTCT TCTACTCGGC TTGCAAAAGA ACCTCCTTGT 1620
CTAGGGTTTT CTCCAAGACG CACCATGGCT GGGCTGTTGC TGTGTTTCCC GAAATTTGAA 1680
CCTCCATATC AGTGTCTGTC CATCATCTGA GACCCCTGGC ACGAGCTGCG GTGGCTCAAG 1740
GCGGGTTTCT TTTCCTGAGG CCAGAAGGGG AAGCGCAGGT AGGGAGTCGT GCCTGTGGGT 1800
ACCGGGAAGC CACAGGTTGC TCAACCTCCC GAGGGGGTAA CCGGGGCTTA CGGTGCAGCC 1860
AGGCCCCCTT 1870