| Tag | Content |
|---|
EnhancerAtlas ID | HS108-13647 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr15:69597380-69598560 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GLI2 | MA0734.2 | chr15:69598030-69598045 | AGCCCACCCACCAAG | + | 6.38 | | ZNF143 | MA0088.2 | chr15:69597476-69597492 | CTGTGCATTGTGGGAA | - | 7.41 | | ZNF263 | MA0528.1 | chr15:69598046-69598067 | AGAGGAGGGAGAGAGGGTGGA | + | 7.22 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_23592 | chr15:69595939-69598665 | Colon_Crypt_1 | | SE_24367 | chr15:69597309-69598217 | Colon_Crypt_2 | | SE_24367 | chr15:69598237-69598633 | Colon_Crypt_2 | | SE_50754 | chr15:69593457-69598718 | Sigmoid_Colon |
|
| | 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 |
| GH15I069303 | chr15 | 69595415 | 69598915 |
|
Enhancer Sequence | GGCTTGGATT CATCATGGTG TCTCAACCTC AGCACTATTG ACTTTCGGTA CCGGATAATT 60
CTGTGTTTGT GGTGGGCGGT GGAGAGGGGG GATGTGCTGT GCATTGTGGG AAGTTAGCAG 120
TAGCCCTGGC TTCTACCCAG CAGACACTGC ACCATCACAT CCCCTTCCCT TCCTGGCAAC 180
CAAAACTGTC TCCAGACATT GCCAAATGTC CTCTCGGGGA CACTCCATCT CTGGTTGAGA 240
CCCCTGGGAT CAATGATCTA TGAAGACCCT CCCAACGGTC ATCCTCAGGA CAGGGGAGAC 300
CATGTTCTCT TTCCAGCCCC TGTTTCATGA ATGTGGACTG GGTGTGAATG AAGACTCAAC 360
ACGTGGGGTG TGCAAGGACT TATGGGTGGA GGGGCCCCTT GGACCTCATG CTGAGAGCCA 420
AGGCCAGTTC TCTTCGCCTT CCAGACCTTG GGTTACATAA GTCGGGGTGG GTGGGGCGAG 480
GCTCGGAGTG AGGGGGAGAG AGGCCTGTGG TTCGGGCCCG CACACTAAGG TCAGTGGCCT 540
TCCAGTGCGG GGCAGCGTGG TGAGTAATCA TCTATTCATG CCCTAGGACT CAGCATTCCA 600
CCCACTTTCC CCTCTCACGC TGCCCTGGGA GGGGACACAG GAAGTGAATC AGCCCACCCA 660
CCAAGCAGAG GAGGGAGAGA GGGTGGAGTG TGGGTGTTGT TAGACGCAAG GGCACGCCTG 720
CGCCGGCCTA CCCTGGGTTT TATTTTGTTT ATTCCTCCCA AGTTAGCTGT TTATTAACTT 780
CGTCCACGGA AACCCCCTTC TGACCTTGTC GCTTAATGGA AGGGCAGACG ATCTTTGGCA 840
GGGGGAGGGG TTTGTTGATG AATATTAGAA GTAAATCACT GTCTCTGGGA ATAACAGACT 900
GTGAGGTTTG GGATAGTACT AACCCAGACC TATTGCTCTG GGGGATTCAT TCCTTCATTG 960
AAGAAACTCT GCTCTGGACT GTGGGCTAGA TGTGGGGCAG GAGAAGGGAA TGAGATATAG 1020
TGCCTGCCTG CAGAACCCCT CAGTCTCAGA GGGAAGACAT GGCTGTCAGG CTGTCCCTGC 1080
AGGGTACTGG GAATGTACAT GGAATGCATG GAGTGGGGTG TGGGCAGCAC CACCCAGCTG 1140
TGTTGCGGGG AATTGGGGGT GGGCAGCTGG GGCAACACAT 1180
|
