| Tag | Content |
|---|
EnhancerAtlas ID | HS098-49987 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr6:134961370-134962790 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr6:134962251-134962270 | TTCTGCCCCCTGGTGCTCA | - | 6.15 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH06I134640 | chr6 | 134961461 | 134961670 | | GH06I134641 | chr6 | 134961689 | 134964507 |
|
Enhancer Sequence | TGGTATTTAT ACACATAGTC AATGGTTATA GTTATGTTTA GCATATAGGT ATCCATTTTC 60
TTTTTCATGG TCACGCTGAG GGACCCTGAT GACACATAGA CCATATTGCC CTTACAAGGC 120
TCTTAATGAC AGAATGGTTG GCATAGCCTT ACTTTCCTAA ATAGTTTGCT GATTCACTTG 180
TTCCATTTTT AGACATCAGC AGATCGGCAT TGGTGACATC TGCTAATTAT TTGGTTTGAC 240
TCGTGACTGG CATGAGACTT CCATCTGCAT CAATCAGTAA GACATGATTA GTGTGAGGTT 300
AATACCACCC AATCCATGAC CAATTTGTTG TAATGAGAAG CCTTGTTTAT TTATCGGTTT 360
TCCCCAGAGG TAATCATTTG TTGGAAACAT AGCTGCCAAA AGTCACATTG TCTTCGTATT 420
AATAGCTTAT CAACTCTCAA ATTGCATTGA CCTACCCAAT TACATATTTA AGACCTTCTG 480
CACCTCTCTT ACGGTTTCCA CCTCTCATTT CTACCTGGAA ACAGTCTTGG AAGACAGCTG 540
AAGACTGTGC TTCTATGGTT CGTCCTTCCT TGTTTCCCTA GTACAATATT TTGAGACATC 600
CCCTCAAATG GCCCTCTTCT TTCTAAACCA TCATCATGTG ACAGTCACAG CTTCATTAAG 660
ACATGTTAGT TACGCTTCCT GGTTTAATTC AGAGTGAATT AAATCATACT CAATAAACTC 720
ACCAAGAGTT TTGTTGGTTT CTTGTGTAAT GCTTGGGTAA GATTAGAAAG GCAATGACCT 780
CCAATCATGG TAGTAGCTAA TTCCTTGTTT AATACTTTAG GTCAAAGTGA GTGCACATTT 840
CACCATTTTG TGGTCTACCA GAGCAAACAC AGAAGAATGC TTTCTGCCCC CTGGTGCTCA 900
TTGTCTGCTA CTGCAGCAGA TGAGTCAGCT GAGATATGTT CCAGACAGAA GCAGAAGGAA 960
TTGTGTCTCT ACTGCTTATA GCACATGAGC AAAGCCACAA CTTTTCAGTG CGTCACATGT 1020
CAGATACCTC CTAAATATGC AAGTGTCAGG GAAATGAATG AAGAGGATCT CTCAATTCTG 1080
TAACAGGAAG CACCACTGGG GAGAATGGCA GAGGCTCTGG GCTCTGGCTC TTGTTGCTTC 1140
ATTAGCCTCT CATCTGGGAG CCCTCTGGGG TGCTGGCTGG TCCACCCTGG CCATGTCTGG 1200
GTCTCTTGAT TATGCCAGGT TATTCCCTGA CTCAACACAC TGACATGTGC TTCTCTCTCT 1260
GCCTAAAAAC TTCCTCACCC CCTTCATCTC CTAAATCGTA TCTCTCCTTC AGAATGTAGC 1320
TGAAGGGCCA CCTTCACAGG AAAGTCTCAA TCAGGACTTC CTTAAATCTT CTCATACCAC 1380
CTGATTCTTC TCCTTCAAGG CACCCATTAC GATTGTAATT 1420
|
