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

TagContent
EnhancerAtlas ID
HS105-74566 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr7:98821850-98822980 
TF binding sites/motifs
Number: 24             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr7:98822667-98822685CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr7:98822717-98822735CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr7:98822659-98822677CTCTTTTTCCTTCCTTCC-6.04
EWSR1-FLI1MA0149.1chr7:98822686-98822704CTTTCTTTCCTTTCTTTC-6.33
EWSR1-FLI1MA0149.1chr7:98822701-98822719TTCTCCTTCCTTCCCTCC-6.45
EWSR1-FLI1MA0149.1chr7:98822671-98822689CCTTCCTTCCTTCCTCTT-6.84
EWSR1-FLI1MA0149.1chr7:98822721-98822739CCTTCCTTCCTTCCCTCT-7.85
EWSR1-FLI1MA0149.1chr7:98822663-98822681TTTTCCTTCCTTCCTTCC-9.07
EWSR1-FLI1MA0149.1chr7:98822709-98822727CCTTCCCTCCTTCCTTCC-9.09
EWSR1-FLI1MA0149.1chr7:98822713-98822731CCCTCCTTCCTTCCTTCC-9.72
EWSR1-FLI1MA0149.1chr7:98822705-98822723CCTTCCTTCCCTCCTTCC-9.93
IRF1MA0050.2chr7:98822650-98822671TCTTTCTTTCTCTTTTTCCTT+6.21
IRF1MA0050.2chr7:98822603-98822624TCTTTCTTTCTCTTTCTTTCT+6.76
Nfe2l2MA0150.2chr7:98822195-98822210TGCTGACTCATTGTG-7.14
ZNF263MA0528.1chr7:98822670-98822691TCCTTCCTTCCTTCCTCTTTC-6.05
ZNF263MA0528.1chr7:98822693-98822714TCCTTTCTTTCTCCTTCCTTC-6.09
ZNF263MA0528.1chr7:98822717-98822738CCTTCCTTCCTTCCTTCCCTC-6.24
ZNF263MA0528.1chr7:98822689-98822710TCTTTCCTTTCTTTCTCCTTC-6.45
ZNF263MA0528.1chr7:98822663-98822684TTTTCCTTCCTTCCTTCCTTC-6.56
ZNF263MA0528.1chr7:98822667-98822688CCTTCCTTCCTTCCTTCCTCT-6.58
ZNF263MA0528.1chr7:98822709-98822730CCTTCCCTCCTTCCTTCCTTC-6.67
ZNF263MA0528.1chr7:98822713-98822734CCCTCCTTCCTTCCTTCCTTC-7.24
ZNF263MA0528.1chr7:98822705-98822726CCTTCCTTCCCTCCTTCCTTC-7.58
ZNF263MA0528.1chr7:98822701-98822722TTCTCCTTCCTTCCCTCCTTC-8.01
Number of super-enhancer constituents: 1             
IDCoordinateTissue/cell
SE_36742chr7:98821449-98823283HMEC
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr79882212598822545
Number: 1             
IDChromosomeStartEnd
GH07I099223chr79882160498823530
Enhancer Sequence
ATTCTTCTAA CAACGGGATT TAGGGCCAGG CGCAGCGACT CATGCCTGTA ATCCAAGCGC 60
CTTGGGAGGC CGAGGCAGGC AGATCACGAG GTCAGGAGTT CGACACCAGC CTGGCTAACA 120
CTGTGAAACC CTGTCTCTAC TAAAAACACA AAAAATTAGC CAGCCATGGT GGCATGTGCC 180
TGGTGTTCCA GCTACTCAGG AGGCTGAGGC AGGAGAATCG CTTGAACCCA GGAGGAGGAG 240
GTTGCAGTGA GCCGAGATTG CGCCATTGCA CTCCAACCTG GGTGACAAGA GTGAAACTGC 300
ATCTCAAAAA AAAAAAAAAA GAGAGAAACG GAGCCATGTC TCAGATGCTG ACTCATTGTG 360
TTATCTTTGG GCAAACTGCT TCACCCCTCC GAGCCCATTT GCTCACCTGC TGAAAAGAGA 420
CCATTACTCA TCTGCCCCAC CCGCCTGCCC AGGCTATTGG AAGGATCAAA ATTAGATTTT 480
GGACTCCGGG GACGTCTGTT TTTATTGTTG TGCCAATGCC AACCCATGAC TCTGGGGAAT 540
TTTTTTCAGC CAGAGGATTT AAGCCCGCTT GATTTCTATA GAAAAACCCA TTAAACTTTC 600
TCCAGATACC ATGAGCCAAT GATTCCATCC AATGCGCTTC TTGCTGCATT TTTAAAGGCA 660
GGGCACTCTG TGTGCCCACT CACTCTTGGG CAGTGCTAGC CACCTGAAAA TTAACCTGAG 720
GCCTTCCCCA AAGCAAACTC CCTCTTCCTT CTTTCTTTCT TTCTCTTTCT TTCTTTTCTT 780
TCTTTCTTCT TTCTTTCTTT TCTTTCTTTC TCTTTTTCCT TCCTTCCTTC CTTCCTCTTT 840
CTTTCCTTTC TTTCTCCTTC CTTCCCTCCT TCCTTCCTTC CTTCCCTCTC GCTCTTTTTC 900
TTTCTTTCTT TCATCTGTTT ATTTTGTTTT GAGATGGAGT CTGGCTCTGC CACCCAGGCT 960
GGAGTGCAGT GCTGGCATCT CAGCTCACTG CAAGATCCAC CTCCTGGGTT CAAGCGATTC 1020
TCCTGCCTCA GCCTCCTGAG TAGCTGGGAT TACAGCACCC GCCACCACAC CCGGCTAATT 1080
TTTGTATTTG TAGTAGAGAT GGGGTTTCAC CATGTTGGCC AGGCTGGTCT 1130