EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS007-10259 
Organism
Homo sapiens 
Tissue/cell
BE2C 
Coordinate
chr20:48982570-48984010 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs6067417chr2048983697hg19
TF binding sites/motifs
Number: 22             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr20:48983073-48983091CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr20:48983077-48983095CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr20:48983081-48983099CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr20:48983061-48983079CCTCCCTCCCTCCCTTCC-7.08
EWSR1-FLI1MA0149.1chr20:48983043-48983061CCCTCCCTCCCTCCTTCC-7.12
EWSR1-FLI1MA0149.1chr20:48983085-48983103CCTTCCTTCCTTCCTTTT-7.95
EWSR1-FLI1MA0149.1chr20:48983065-48983083CCTCCCTCCCTTCCTTCC-8.13
EWSR1-FLI1MA0149.1chr20:48983069-48983087CCTCCCTTCCTTCCTTCC-9.42
IRF1MA0050.2chr20:48983319-48983340ACACAGTTTCATTTTCACCTT+6.64
Stat6MA0520.1chr20:48983524-48983539GTTTTCCAGAGAAAA+6.07
ZNF263MA0528.1chr20:48983056-48983077CTTCCCCTCCCTCCCTCCCTT-6.14
ZNF263MA0528.1chr20:48983081-48983102CCTTCCTTCCTTCCTTCCTTT-6.16
ZNF263MA0528.1chr20:48983043-48983064CCCTCCCTCCCTCCTTCCCCT-6.46
ZNF263MA0528.1chr20:48983042-48983063TCCCTCCCTCCCTCCTTCCCC-6.61
ZNF263MA0528.1chr20:48983069-48983090CCTCCCTTCCTTCCTTCCTTC-6.76
ZNF263MA0528.1chr20:48983073-48983094CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr20:48983077-48983098CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr20:48983039-48983060GTCTCCCTCCCTCCCTCCTTC-7.12
ZNF263MA0528.1chr20:48983065-48983086CCTCCCTCCCTTCCTTCCTTC-7.19
ZNF263MA0528.1chr20:48983061-48983082CCTCCCTCCCTCCCTTCCTTC-7.38
ZNF263MA0528.1chr20:48983052-48983073CCTCCTTCCCCTCCCTCCCTC-7.65
ZNF263MA0528.1chr20:48983048-48983069CCTCCCTCCTTCCCCTCCCTC-7.73
Number of super-enhancer constituents: 6             
IDCoordinateTissue/cell
SE_28491chr20:48982335-48987321Fetal_Intestine
SE_31629chr20:48983043-48983874Gastric
SE_33764chr20:48982789-48984100HCC1954
SE_52401chr20:48982681-48987083Small_Intestine
SE_53316chr20:48982599-48984069Spleen
SE_56118chr20:48982851-48984157u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr204898308348983800
Number: 1             
IDChromosomeStartEnd
GH20I050365chr204898243148987174
Enhancer Sequence
CAATCTTTTT TGTCTTTTCT AATCTGATAG GCAGAAAATG ACATATCATT GTAGCTTATC 60
ATTGATAACT GGTGGGGTGG AACTTGTCTT CATACTTTTT TTTCTTTTTT TCTGAGGCAG 120
TGTCTCCCTT TGTCTCCCAG GCTGGAGTGC AGTGGCACCA TCTCAGCTCC TACATCAGCC 180
TCCCAAGTAG CTGGGACTAC AGGCATATGC CACCACACCT GTCTAATTTT CCTTATTTTT 240
TGTAGAGATG AGATCTTTCT GTGTTACCCA GGCTGGTCTT AAACTCCTGG GCTCAAGCAA 300
TCCTTCCACC TCGGCCTCCC AAAGTGCTGG GATTATAGGC ATGAGCTGCC TCGCCTGCCA 360
GAATAGTGGG TTTTTAATAC GGTGTTTACC TCTTCTTATT GTTTTGCAAG AACTCTTTGT 420
ATATTAAGGA TAGTAATTCT TTCTAAGAGT CTTATAATTG ACTATAAAAG TCTCCCTCCC 480
TCCCTCCTTC CCCTCCCTCC CTCCCTTCCT TCCTTCCTTC CTTCCTTCCT TTTGTTCCCT 540
TCTGCTTTCT AAGGATATGC CTGGTGTTTG GCAAGCATTG CATGAATTAC ATTAGGAAAT 600
AACTTTTGTA ACAAACCCAT TTAACAACCA TTCTTTGTTC CCCGCCTCCT GATAATGCTC 660
AGAGCCACAG CAACAGCCTT TGCCCAACTC CATGTCATTA ACCCTTGATC TTTTCCTGCT 720
GAATAGCAGA TTGCTTTCCG GGGCTGGCAA CACAGTTTCA TTTTCACCTT CCTGCTGATG 780
GAACTGCCCT GGCTCTGTGC CAGATGGCTG TTTACATAAG AAATGATTTG ATTATATTGC 840
ACAGCCAATG GCAGCCTTTC TCAGAATAAA GAAGCCAGAA ACATATAATC AAAGCCATTA 900
ACTGTGTACA AAGAAACGCA GCCCACTCTA AATTTCCCAC CAACCATAAT CACAGTTTTC 960
CAGAGAAAAA TAAGAACAGG GTTATGGTTC CCTACTAAAA ACGTGTTAGG GGAAAGACTT 1020
TTAAAAGGAA ATTGTGGTAT AGCTCAGTTG CACTCTCAGA TCAACCCTTG AGCCTTGACT 1080
CCAATCCCAG CTCTGTAACT CACTGTCCTT GTGACCTTGG AAAAGTCGTT TACTGCCAAA 1140
AGCCTCCGTT TCTTTATTGT AAAATGGCTA TAATAGTAAT ATCAACCTCA GAGGTTTACG 1200
AGAGGATTAA GTGAGATAGT GCATAAGAAC ACTTTCTCAG TCAGAATGTT TTCAGCCGCA 1260
AGGAGCAGAA CACTTGACTA AAGGAGGGAA AAAAAAGCTA GAGGACTTAT AATTTTATTT 1320
AACAGGGTTG TTTCATTTGG AGGCATAAAG ATGTAACCAG TGATTCACAT TCTTTTCTTC 1380
TTCCTGCTAT GCCATTCTCA GCAATTTATG GACATGTCTC CTCATGGTTT CAAGACAGCT 1440