| Tag | Content |
|---|
EnhancerAtlas ID | HS176-15740 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr16:89908810-89910120 |
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 | | Nr2f6(var.2) | MA0728.1 | chr16:89908839-89908854 | TGAACTCCTGACCTC | - | 6.22 |
|
| | 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 | GGGTTTTGCC ATGTTGGCCA GACTGGTCTT GAACTCCTGA CCTCAGGTGA TCCACCCACT 60
TCGGCCTCCC GAAGTGCTGG GATTACAGGC GTGAGCCACC GTGCCCGGCC GTGAACATTT 120
AATTTTGATA CAACTTTTTT TGTTAACCTA TGGAGTATTT GAGCCAGAGG CACAAACATT 180
AAAATTATTC CAACCAGAAG CTTCCCATGC ACTGAGGACC TCGCCTGATG TGGGCTTAGT 240
CTGTGAAGGC ACTGAAGGGC CAGCCGGCCA CCAGTCAGCC CTTCCCCACA GGGCCCTGGT 300
CTGTTCCAGG GAGCACCTTT GTTTGGGTCT GATGTCTTCC ACCTTCCCAT GGCCTCGGCC 360
CAATCACAGC TGCAAACGTG CTGAACGCCC AGCGCGGGCC AGGACTGCCC AGGCCCTGGG 420
GACCCACACC CCCACCGTGG GCCACACATT GTTCTATGAA CTCCACTGAT GCGGGGGTGG 480
ATTGCTTTCC ATTATGTTAA TGGAGCAGGC TCCCTTTATC TTTGGCAATC TTCCTGGTTC 540
TTGATGGCAT TTTGAAAATA TTTGTGGAGT TAGCAGGTCC ACTGAGCAGA TGATTTCATG 600
GCTTAGATAT AGACGCATAT ATACATCTTA CCTCATTCCA GAAAGAATTC CAGGCAGCTG 660
GAGCTCTTGT TCTAGCACAG TCCCACCTGC ATGCCCAGTT CAAGGAAGGC TGTAGAATCG 720
GGTGGATGTT TTGCATCCCA CCCAGCGCAG CATCTTGGGA ACCCCGGGGG AGGAGGGTTG 780
GGGAGCACAG ACCCTGGGCC CCACGGCCTG GCCCCACTCC TGGCACTTAT CAGCCCTGAT 840
ACCTTGGAGC AAACAGATTC ATCCTCCGGT CTCTGTTTCC TCATCTGTGA AACGGGAAGT 900
GGAGCAACCA GCTCCAGCGT GAGCACCGGC AAAAGGCAGG TTCGCTCCCG GGCCTCCCTC 960
AGGGCCAGGT TTCATCAATG AAATACGTGA CTCCAGCTTC CACCTGCATT TCCACTCGGA 1020
CTGTGGTTCT CTAAGAGGCA TAAACAGTCT TGGGGGGACA TCTCCAAATC GGTGGTCTCA 1080
GTCAGATGCC GACTTACCTG CTCTGCAAAG TCTGTCTCTC CCTCTGACCC GGGGTTTCTC 1140
ATCTGACTGC TGTGATTTCA GTGTGCACAA CCTCAGTCCC AGGCAGGTGG TGTGTCTCAT 1200
CTCAGACCAC AGGTTCTTTC CTGAAGATGT GCCTCGATGG ATGGAGCTGC TGCCTTGCTG 1260
CCACGTTTTT TTTTTTTTGT TTGTTTTTGT TTTTTGTTTT TTTTTTTTTT 1310
|
