| Tag | Content |
|---|
EnhancerAtlas ID | HS133-26543 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr6:25963510-25964330 |
Target genes | | Number: 38 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr6:25964092-25964113 | TTCTCCTTTCTCTTTCTTTTG | + | 6.52 | | SPIB | MA0081.2 | chr6:25964277-25964289 | CACTTCCCCTTT | - | 6.07 | | ZNF263 | MA0528.1 | chr6:25963608-25963629 | GGGGGCGGGCGGGGGGGAGGG | + | 6.41 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28528 | chr6:25961758-25965193 | Fetal_Intestine | | SE_29180 | chr6:25961786-25966025 | Fetal_Intestine_Large |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 25964007 | 25964200 | | chr6 | 25963800 | 25963815 |
|
Enhancer Sequence | GTAATTGTAG TTAAATTACT GTTTTTTATT CTAGGCACTC TTCAAACTTC CTCCTGACTC 60
TGCCCCTGTC CTAGAGGAGC TCCCAGGAGT AGGGGTGTGG GGGCGGGCGG GGGGGAGGGA 120
TCGGGGGTAC AGGGAGAGCC CAGCTAGGTT CTCAGAAGAG GCAGGCTTTT TCGCTCCTGG 180
TCACTCCTCT GTTGCCTATC CCTGGCCTCC CCCATCTTCT TTCTGCCTTC CCTACCTCCT 240
TGGGTCTGCA AACTCTTTAT GTTGCAATCA CTCTGAACAT GTCTCTTGAG ATAGGTCCTG 300
TCCTGGAGAA GAGATAGTAA AAGTAAACTC CCCAGTTCTG CAGGAGCTCT GATCCCATAG 360
AAATAACTGC TCCTCAGGAG CAAACCCTCT GCTCTGCAGC CTTCTTTCCA ATTCTTATTC 420
CCTCAGTTTA GGGAGAGGGC ACAAAAAGGA TAAACCGGTT CTTCTGGTTG TTCTGGTTGC 480
CTTGATTGCT TCCATTATCC TCCTGGTTGG GTCTCTAGCA AGACGTTATT AGCCAGGGAA 540
GTCCCACTTA GGCACCCCTC TCTGCAGAAG AGGTATTCAC TATTCTCCTT TCTCTTTCTT 600
TTGCCTATTA TACCTCTGCT CCTGAAAGCA AAAACAACAA CAACAAAAAC ACAAACAAAA 660
AACAACCGAC CTTATTAACC AGTGTTGGTT GTTGTTCTTT GTGGGGGATG GGGGGGGTCG 720
AGGTGGAGTC AAATTTTATT GTCATGATGG TGTAGGAGCC AAGGGAACAC TTCCCCTTTG 780
CCTTCTGAAG TTCACTGAAA AATCGACTCA CAAAAGGCAG 820
|
