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

TagContent
EnhancerAtlas ID
HS028-00785 
Organism
Homo sapiens 
Tissue/cell
Colo829 
Coordinate
chr12:13052430-13053520 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr12:13053459-13053480CTCCTCTTCCTTTCCTCCCTC-6.43
ZNF263MA0528.1chr12:13053499-13053520TCCCTTCCCTCTCCCTCTTCC-6.4
ZNF263MA0528.1chr12:13053466-13053487TCCTTTCCTCCCTCTTCCTCT-6.5
ZNF263MA0528.1chr12:13053206-13053227GAATGAGGATGAGGGGGAGAA+6.78
ZNF263MA0528.1chr12:13053212-13053233GGATGAGGGGGAGAAAGAAAG+6.81
ZNF263MA0528.1chr12:13053463-13053484TCTTCCTTTCCTCCCTCTTCC-6.92
ZNF263MA0528.1chr12:13053209-13053230TGAGGATGAGGGGGAGAAAGA+7.14
Number of super-enhancer constituents: 10             
IDCoordinateTissue/cell
SE_02173chr12:13051911-13053728Aorta
SE_23547chr12:13052684-13053623Colon_Crypt_1
SE_28138chr12:13052808-13053649Fetal_Intestine
SE_28922chr12:13051231-13057938Fetal_Intestine_Large
SE_34394chr12:13052411-13053680HCT-116
SE_36163chr12:13051744-13055812HMEC
SE_38847chr12:13051287-13055917HUVEC
SE_57272chr12:13050050-13053678VACO_400
SE_58021chr12:13052873-13053228VACO_9m
SE_64427chr12:13051485-13053710NHEK
Number: 1             
IDChromosomeStartEnd
GH12I012897chr121305030913057779
Enhancer Sequence
GAGCTATTCT TTCTGACCAT GTGACACTGG ACATGTACCT TCCTCACTCT GTTAGGTTTC 60
TCACCTATAA AATGGGCTGT AGGAATGTTA AATGAGGTAA TGGATGTAAA AGCATGTAAA 120
TGAGAGAATA TGTGTAAAAA TACATAACTA CTCAGCATAG TGCCTGACTC ATAATAGGAC 180
TCAGGAGGTG ACAGTAGCTG TCATTATTCT TACTCATAAT TACATCATGA CTGTTATTAC 240
TACTGACTGA ATGTAGCAAT TCGAGAATAG AGAAAAAATG AAAATGCTAG AAAGTCACAC 300
ATTTTCAGGG CTGGGCTGGC GCGAAGACAC ATTTTGACAG AATGAGAGAA ATCTCATAGG 360
AAGGAAGACA AAGTCAGTTT GTCTTTGCAA GGTTCTGGGC CCCAGATGAT TCATTCTCAG 420
ATGCTCTGGG AAGGACTGCG TAGAATAAGC ATGGGCAAAC TTCCAGGCCT AGTCACAAGC 480
AACTCTACAC ACTTTCCCCA TCTCTCTGGT TGCGAAGAGG AGTCTCAGGT TAGAAACCCA 540
AAGCGGGAGA CTCATCACAT GTTCACGTTT TTCCCTGCAC AGTGGTCAGT GCTGTGTGTC 600
AGTCAAGGCC ATGTCTAGGG TCAGCGCTGC TCCAGGAGCC TCTGGCTTTG TCCTTCAGGT 660
GGGCAGTCCC TTGCTGTGTC TCTTCTTCAG ACCCTTCAAC CTTACCTCTA GCCCTGGCTT 720
TTAGTTTGGG TAGGAGTTTG TGGCACATAC TCTTTTAATG ACAGGAGATG GGGCAAGAAT 780
GAGGATGAGG GGGAGAAAGA AAGACATCTG GAAGTTTTGT ACATGAAGCT CCCCAGGTGG 840
GTGAACGGTG GAGCTGAACA TGAGTTCAGA CCACGTAGTT CAGCAGCGTG TCCTGCATTT 900
TATAGATGAG AGGAGGCTTT GAGAGGTCAA GTGACTTACT TGTTCACACA GCCTGGCAGC 960
TGAAACCCCT TCTCCCTAAA GGGGAGGAGG AACAGAGGGC TTGGAGTTGA CCCAAGAAAT 1020
GACTTCGCCC TCCTCTTCCT TTCCTCCCTC TTCCTCTTGT TCTTATTCTT CCCTTCCCTC 1080
TCCCTCTTCC 1090