| Tag | Content |
|---|
EnhancerAtlas ID | HS184-12942 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr16:89908910-89910100 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GFI1 | MA0038.2 | chr16:89909957-89909969 | TGCTGTGATTTC | - | 6.22 | | Gfi1b | MA0483.1 | chr16:89909957-89909968 | TGCTGTGATTT | - | 6.62 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_23295 | chr16:89909425-89910097 | Colon_Crypt_1 | | SE_24794 | chr16:89908977-89909411 | Colon_Crypt_3 | | SE_35059 | chr16:89908590-89910178 | HeLa |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I089842 | chr16 | 89908770 | 89910250 |
|
Enhancer Sequence | GTGCCCGGCC GTGAACATTT AATTTTGATA CAACTTTTTT TGTTAACCTA TGGAGTATTT 60
GAGCCAGAGG CACAAACATT AAAATTATTC CAACCAGAAG CTTCCCATGC ACTGAGGACC 120
TCGCCTGATG TGGGCTTAGT CTGTGAAGGC ACTGAAGGGC CAGCCGGCCA CCAGTCAGCC 180
CTTCCCCACA GGGCCCTGGT CTGTTCCAGG GAGCACCTTT GTTTGGGTCT GATGTCTTCC 240
ACCTTCCCAT GGCCTCGGCC CAATCACAGC TGCAAACGTG CTGAACGCCC AGCGCGGGCC 300
AGGACTGCCC AGGCCCTGGG GACCCACACC CCCACCGTGG GCCACACATT GTTCTATGAA 360
CTCCACTGAT GCGGGGGTGG ATTGCTTTCC ATTATGTTAA TGGAGCAGGC TCCCTTTATC 420
TTTGGCAATC TTCCTGGTTC TTGATGGCAT TTTGAAAATA TTTGTGGAGT TAGCAGGTCC 480
ACTGAGCAGA TGATTTCATG GCTTAGATAT AGACGCATAT ATACATCTTA CCTCATTCCA 540
GAAAGAATTC CAGGCAGCTG GAGCTCTTGT TCTAGCACAG TCCCACCTGC ATGCCCAGTT 600
CAAGGAAGGC TGTAGAATCG GGTGGATGTT TTGCATCCCA CCCAGCGCAG CATCTTGGGA 660
ACCCCGGGGG AGGAGGGTTG GGGAGCACAG ACCCTGGGCC CCACGGCCTG GCCCCACTCC 720
TGGCACTTAT CAGCCCTGAT ACCTTGGAGC AAACAGATTC ATCCTCCGGT CTCTGTTTCC 780
TCATCTGTGA AACGGGAAGT GGAGCAACCA GCTCCAGCGT GAGCACCGGC AAAAGGCAGG 840
TTCGCTCCCG GGCCTCCCTC AGGGCCAGGT TTCATCAATG AAATACGTGA CTCCAGCTTC 900
CACCTGCATT TCCACTCGGA CTGTGGTTCT CTAAGAGGCA TAAACAGTCT TGGGGGGACA 960
TCTCCAAATC GGTGGTCTCA GTCAGATGCC GACTTACCTG CTCTGCAAAG TCTGTCTCTC 1020
CCTCTGACCC GGGGTTTCTC ATCTGACTGC TGTGATTTCA GTGTGCACAA CCTCAGTCCC 1080
AGGCAGGTGG TGTGTCTCAT CTCAGACCAC AGGTTCTTTC CTGAAGATGT GCCTCGATGG 1140
ATGGAGCTGC TGCCTTGCTG CCACGTTTTT TTTTTTTTGT TTGTTTTTGT 1190
|
