| Tag | Content |
|---|
EnhancerAtlas ID | HS076-47127 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr6:3013310-3014540 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAFF | MA0495.3 | chr6:3013914-3013929 | GTGCTGACTCATCAG | - | 6.22 | | MAFF | MA0495.3 | chr6:3013914-3013929 | GTGCTGACTCATCAG | + | 6.3 | | NFE2L1 | MA0089.2 | chr6:3013913-3013928 | AGTGCTGACTCATCA | - | 6 | | NFYA | MA0060.3 | chr6:3014231-3014242 | TCTGATTGGTT | - | 6.62 | | NFYB | MA0502.1 | chr6:3014232-3014247 | CTGATTGGTTCAGAT | - | 6.81 | | Zfx | MA0146.2 | chr6:3013432-3013446 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_10010 | chr6:3012114-3014720 | CD14 |
|
| | 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 |
| GH06I003013 | chr6 | 3013881 | 3014030 |
|
Enhancer Sequence | TCCCGAGTAG CTGGGACTAC AGGCGCCCGC CACCACGCCC GGCTAGTTTT TTGTATTTTT 60
AGTAGAGACC GGGTTTCACC GTGTTAGCCA GGATGGTCTC GATCTCCTGA CCTCGTGATC 120
CACCCGCCTC GGCCTCCCAA AGTGCTGGGA TTACAGGCGT GAGCCACCGC GCCCGGCCGA 180
TGTAACACTA CTTTAAACAC TTTACCTAAT TGGGTAAAGA TATCCACGTA GCCAATATCA 240
CTCACTCCAA ATCCCGACTG CCATGTAAAT AGGAATGAAG GATATTTCCA TTATTCCAGT 300
GGTCCAAGAA TCATCTGAAA CCTGCCAGTC TTGTTGCTTC CCTTCTCTTC CCGTTCCTGC 360
CCTGAGACAT TCTGGGGCTG CTTGAGAACC ACATTTATCT GCACAAATGT TTATCAGGGT 420
AAATCAGGCC AAATGCATCT CCTTAAATAT CCTGCCTTAA ATATCCTGAT CATTAAGAGG 480
AAAATCTCTG GTTTCTACCC TCTCAGTGGT TGCTTCACCC CCAGCCCAGC CACCTTCCTG 540
TATTTGTTCA CAAGGAGGTG ATGCCACTGC AGAGTGAACT GGCCCAGCAA AATGCCCTCC 600
AGGAGTGCTG ACTCATCAGG CCACTTCCCG CCACTGCAAG GAAGATGTGC AGGCATGGCT 660
GTGGCTGTGT AAACCTGGCA GCAGAGTACG CACATGAGCT TTGAGGGAAT TGTTGGGTGA 720
CAGAAATTCC TGTCCAACTA GAAGGAAAGG GGAATCTATT ATAAGGGCTC TGGTCACTTG 780
GGCCTCCTGG ATCCCAAGGA CAGAGCTGTA GCTGCTCTCG TCCACAGATT CCCATCTGCT 840
CCTTTCTGCC TCTTGGCTCT GTTCTCTCTC ACTGCTTGCC AGGGACTGGA TCCCCTAGAT 900
CCAGAATTTC CAACCAAGGG ATCTGATTGG TTCAGATCAT TTCTGTTTTC CAACCCTGCT 960
TGAGGATGCG GAGTGGGCAG GAGAACGAGA GCACTGTTCG CATGAGTCCG CCATGTGAGG 1020
GCAAGGCAGG GGGTGAGCGG CATGTGACCA CTTTCCAGAC AAAACCACCT TTCCAGAATG 1080
ATGAGGTTCC CAAGCCTTCA TAAAAGCAAC CTGCATGTGC GGGAAGAGGG CTGCCTCATC 1140
CCTGCCCAGG CTTGCCTCTG CACACCCCTT CCCGACACCA GCCCTTTCTT TACTCAGTGA 1200
CCTTGAGCTG CTAATCTGAC CAAAGTGCAG 1230
|
