EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-36941 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr22:36828020-36830140 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs28430325chr2236829002hg19
TF binding sites/motifs
Number: 20             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr22:36830092-36830110TCTTCCTTCCTTCCTTCC-10.05
EWSR1-FLI1MA0149.1chr22:36830096-36830114CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr22:36830100-36830118CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr22:36830104-36830122CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr22:36830108-36830126CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr22:36830112-36830130CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr22:36830116-36830134CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr22:36830120-36830138CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr22:36830084-36830102CATTTCTTTCTTCCTTCC-6.81
EWSR1-FLI1MA0149.1chr22:36830088-36830106TCTTTCTTCCTTCCTTCC-8.26
Myod1MA0499.1chr22:36828940-36828953GGCAGCTGTCCCT+6.48
ZNF263MA0528.1chr22:36828789-36828810TAAGGAGGAAGGGGCGGAAGC+6.07
ZNF263MA0528.1chr22:36830088-36830109TCTTTCTTCCTTCCTTCCTTC-6.36
ZNF263MA0528.1chr22:36830096-36830117CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr22:36830100-36830121CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr22:36830104-36830125CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr22:36830108-36830129CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr22:36830112-36830133CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr22:36830116-36830137CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr22:36830092-36830113TCTTCCTTCCTTCCTTCCTTC-7.03
Number of super-enhancer constituents: 16             
IDCoordinateTissue/cell
SE_23071chr22:36828875-36830123Colon_Crypt_1
SE_23740chr22:36828926-36830116Colon_Crypt_2
SE_24731chr22:36828512-36830098Colon_Crypt_3
SE_27650chr22:36827998-36832917Fetal_Intestine
SE_28644chr22:36828082-36833066Fetal_Intestine_Large
SE_31378chr22:36828245-36830137Gastric
SE_37504chr22:36827729-36830560HSMMtube
SE_42094chr22:36828136-36830059Lung
SE_47757chr22:36828247-36830123Pancreas
SE_50050chr22:36828019-36830169Sigmoid_Colon
SE_52340chr22:36828055-36830122Small_Intestine
SE_53283chr22:36827843-36830121Spleen
SE_58448chr22:36724049-36832686Ly1
SE_62151chr22:36773097-36852649Toledo
SE_63127chr22:36801020-36866853Tonsil
SE_65459chr22:36828169-36830241Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr223682832836830089
Number: 1             
IDChromosomeStartEnd
GH22I036431chr223682804036832971
Enhancer Sequence
AGCCGTGCAT CTAGTCCCAG CAACTCAGGA GGCTGACGCA GGAGGATTGC TTTAGGCCAG 60
GAGTTGGAAA CCAGCCTGGG CAACCTAGTG AGACTCATCT CTACAAAACA AAAAAGCAGG 120
AACTCTGGAG TCCAAATACT GGTCCCTGCA CTTATCTGCT GTGTGTCCTT GGACAAGTTA 180
CTTACCCTTT CTGGGCTCTG GCCCCTTCAT CTGTGATATG GGGGTATCGT GGTAGCACAA 240
TCACAGCGCT GTGTGAGGAA TAAATGGGAG TCCTCACATC CGGCCTGTAG CAGCGCCTGA 300
GCCCCGGCGC ACACCCCCCA GGCTCACTGT TTACTTCCCA CAGCATAGAT GTGGGCCCTC 360
CTGGAGGCCA TTTCTGATAC CCTACATCCT ACTTCTCCGC CCTGCATCCG ATCCATAAAC 420
CCTCATGGAG TGCTCCCCGG TGCCAGGCTG GACTAGACAT GATGCGGAGA CTAGCAGGAA 480
CCAGACAGGG CCTCCTCTGG GAGCTCTGAG ACAGGAGCTC AGAACCCTGT GCGGGAAGCC 540
CCAGGAACTT GCTCTTGAAC ATTCTCGGGC TCCCCAAGGC CTCCTTCCCT GGGAGCTGAA 600
TGAATTGGCC TCACCTGCCA GTCCCCAGGT GACCCCCGGG AAGGAGCTGA GAGCCTGGGA 660
CGGGTGCTGG GTTCCTTCTT CATTTTGTTC CTCTGGGTCT GTCCCTGTGC TGAGAAGAAT 720
GGCCCCTGGC CCTCTTAACC CAGGAATGCT GAGCATTTCT TAACACCACT AAGGAGGAAG 780
GGGCGGAAGC TTCCTCCCCC AAGCTCTAGA AGGATCCAAA TTATTTGCTA AAACCACAGT 840
CCAGGCGAGG TCTGGGCAGA TGGGGTTCTC AGAAACCAGG CAGAGATTCT GGCTCCGATT 900
ACTCTGTGGG GAGCGGGAAG GGCAGCTGTC CCTAAAAAGG AAAATTAGCC ACGCATGGGG 960
GTGGATGGAT GGAGGTGAGA CCGGAAAAGA ACTCTTCTCC GCAGGGCTGT GGGGCTGCCC 1020
TGGACATGCA TGGGCAGCTG GTCCTCCCAG CCCAGGCCCC TTCTCATCCC ACTCCCTACT 1080
CCAGGTCTCC ACCAGGTCAT CCTTTTCTCT CTTCCCAGGC CTTATTTGTC AAATGCCTCT 1140
TTCTAGGACC TCTGTTGGCT GGAGTCTGGT CTCAGATCAT TCATTCCATA GCTATTTACT 1200
ATGCGCCAGA AGCTGCACTC ACTGGGGGTC CAGGCAGCTC AGGGACGGGG ACAGTGTGCT 1260
TCATGCGGGC AGGAGCTATG TCGTGTCTTC CGTGGTGTCC CCAGGGCCTG GCTCAGCGTG 1320
GCCACAGGCT AGACACAGGA GCAGGACTTG GCAGGGTTGG CCCGGCTTTC CCAGCACCTC 1380
CAGGCCCACT CTTTGTCCTC ACCTGCATCC CACGGCTCCT TCCTCTCCCC GTCCCTTCCC 1440
CAGCTCTGCT CCCCCAGCCC CCACTCCCCT GTTTGCTCAG CTGCCTGTGG GGGCCTGCAC 1500
TCCACCTCCA CTGGGCCCAC AGCCAAGGTC AACAGGACCA GCCTCCTGGC CCTGGAGATG 1560
TGGGTGCAAC ACAGGCTCCA ACTGAAGGGC ACCAGACTCC CCGGACTATT CCTGGGCCGG 1620
CTCTCCCCTA CCCACCTCCG CCACATTCTG AGTGGTCTCC CAAATACAGA CCCAGGAGGC 1680
CAATCTCCTG GGCTCCTGTA TCAGTCAGGG CTTAACCAGA GAAACAGAAC CTGGAGGAAA 1740
TATAGAGGCA GAGATAAAGA TGGACAGATA GATTGCAAGG AATTGGCACA TGTGATTGTG 1800
GGGCTGGCTG GGAAAGGCTG ACAGGTGCAG GCAGGCCAGC GGGAGGGGCG GGCTGGGGCT 1860
CAGGCAGGGA CTGAAGCCGC TGGCCGTAGG TGGAATTTCT TCCCATCTCC AGATTCCTAA 1920
CTCCGTCACA TCTGCAAAGT CCCTTTTGCC ATGTAGGTTA ACACATTTGC AGGTTTGCGG 1980
GATCAGGACA TGGACATCTT TGGGTCATTA TCTGGCTCAC CGCAGCCCCA GAGGGCCTAC 2040
TGCCCTTCCA TTTGTTCATT CACTCATTTC TTTCTTCCTT CCTTCCTTCC TTCCTTCCTT 2100
CCTTCCTTCC TTCCTTCCTT 2120