| Tag | Content |
|---|
EnhancerAtlas ID | HS118-12329 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr22:47041950-47043280 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MNX1 | MA0707.1 | chr22:47042917-47042927 | TTTAATTACC | - | 6.02 | | PPARG | MA0066.1 | chr22:47043073-47043093 | AGTGGGTGACCCAGACCTAC | - | 7.38 |
|
| | Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
| SE_23756 | chr22:47041976-47042426 | Colon_Crypt_2 | | SE_24734 | chr22:47041815-47042491 | Colon_Crypt_3 | | SE_26636 | chr22:47041960-47042808 | Esophagus | | SE_28507 | chr22:47040818-47044070 | Fetal_Intestine | | SE_31503 | chr22:47041929-47043786 | Gastric | | SE_40615 | chr22:47040847-47044155 | Left_Ventricle | | SE_50122 | chr22:47041245-47043893 | Sigmoid_Colon | | SE_52376 | chr22:47040862-47044086 | Small_Intestine | | SE_65411 | chr22:47041120-47042764 | Pancreatic_islets | | SE_65411 | chr22:47043034-47044291 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I046645 | chr22 | 47040946 | 47043883 |
|
Enhancer Sequence | TTGCTAGGCT GTGTAGGGGA GCCCTCGTGA CTGCCTTTCT TCTTCCTGTG TTGCTGGAGA 60
GGGCTGCAGA TGCCTCCCTG GCTGAGCTGG AGGGTGCTCC CCTAGGCTAC CACGCCCTGT 120
CTCTGGGCAT GGGTACCCTC GTAGCGCCAG ACACGGGTGG ATTCCCGGCA GATGCACTCA 180
CACGGGCAGT GGCAGTGGTT CCTCAAGAGT GTGACTTGGA GAGAGACTGC CTTTTCCTCC 240
TGAGCCCCTG ATGCTCCCAG AAGCTCCCTT TCCTGCTGTG ACATACAGGG ATCAGAGTGG 300
CTGGCCCTTA CGCCATGGGA GATCTTCTCG AAGAAGCTGG CAGGAGGGGC TGGCCATCTG 360
CTTCCTGAGG CCTGCAGACC TTCCTCTGAA TGCTCAGTTT TAATGGAGGG GTCCTGGAGC 420
GGAAGGGAAG TTTCTAGGTG GCTGTCCTGG GTGATTCAGA GTGAGGAAGA CCTTCCTTAC 480
CATTGAAGTC TTCTGGAAGC AGAAGGGTCT GGGGAGCTGC CAGCTCCCTG CTGGCGGGGG 540
TGTCCTTTTG AGGCCTGATG GAGACAGGCT TAGGTGTGGG GTTGACTCAG TGTCCCTGGA 600
CTTGCCCCTT TGGACCTGGG CCTGTGGGTG TGGTTCTTGG CTCAGGCCTT TTAAACTCTG 660
CTCTTACAGT TTCTCTGGTG GTGAAAAGCT AAACTCTGTG TTAGTGTGTT TTCACGCTGC 720
TGATAAAGAC ATACCTGAGA CTGGCGCTTT ACAAACAAAA GCGGTTTAAT GGACTCACAG 780
TTCCACATGG CTGGGGAGGC CTCACAATCA TGGCGGAAGG CAAGGAGGAG CAAGTCACAT 840
CTTACCAGAT AGCAGCAGGC AAAGAGAGAG CTTGTGCAGG GAAACTCCCC CTTATAAAAC 900
CATCAGATCT CGTGAGACTC CTTCACGATC ACAACAAGAA CAGCACAGGA GAGACCTGCC 960
CCCGTGTTTT AATTACCTCC CACGGGGCCC CTCCCACAAC ACTTGGGAAT TCAAGATGAG 1020
ATTTGGGTGG GAACACAGCC AAACCATATC AGACTTCCAG GGCCAGACAC TGGGTTGGTC 1080
TGGTTCTGCC CTAGAGTGAC ATGTTTAATA AGTGACGACT GTGAGTGGGT GACCCAGACC 1140
TACAGAAGGG AGCAGACAGG CAGAAGATGA AGACAGGTGG CACTGATACA GCAGCGTGTC 1200
TATATTATAT GGAATTTCCC TAGGAAAAAA TGAAGTTGGC CCCCAATCCC TGTTTCTCCA 1260
TCACCTCCAT TGCCCCATGA ACTCCTGTCT GCTCTTTAAT TACACATTGT GGATGTTTGG 1320
CCCTGGGATA 1330
|
