| Tag | Content |
|---|
EnhancerAtlas ID | HS133-08438 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr13:30435300-30437130 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr13:30436580-30436601 | TTCCCTCTATCTCCCTCCTTC | - | 6.6 | | ZNF263 | MA0528.1 | chr13:30436589-30436610 | TCTCCCTCCTTCCCTTCCCTC | - | 6.7 | | ZNF263 | MA0528.1 | chr13:30436556-30436577 | TTTCCCCTTCCCTCTTCCCTC | - | 6 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I029861 | chr13 | 30435205 | 30437062 |
|
Enhancer Sequence | CAAATTGGGC CTGGGAATTT GAACCCCAAA CTGTAACTTT AGGGCCACTT ACTTCACAAA 60
GAAAAGGGAT CAAGTAAAAA ATTTCACACA TTTGTATCCA TTCCCTTACC CGTTGCTGTC 120
CACACTTACT CTGACCTCAT CACCCTCCTG CTTCAGGGAA GCCCTATCCC CCTCCCTTCT 180
AAAACCCTCT ACCTGCCCCA TAGCCACTCC CTCTGTCTCC AGAATCTTAT TCTGACAAAC 240
AATCCTTCCA TCTCTTACAT CTTCTGTCTC CTGCTCCCAG GGTTCTCCTA CCTATGGGGG 300
CCATATAATA TATTGTCCAA ATCAGGAAAT ATTCACGGGG AAATGGTACT ATTAATCATT 360
CCTAGCAACA ACAGGTAAGT TGGGGCTACC CCAGGCAAAC CAAGCTTCTT CTCTTCAGAG 420
TGGAAATAGG CTCAAGCCTC TCCCATCTTG AAAAACAGGG CCTTCTCATT TCTCAGTGCT 480
CTTGCTCTAA CTCCTACCCT CTCTTGTTCT TTCCCTTAAC ACCACACTTC TTCAAAGTAT 540
GTGGGAGCGC CTCCTCGGTA CTCCATGTAA CCCTCAGGCA GGGCTGCTGC AAAGGGCTAT 600
GCAGACTGTA CACAACATAA CTCCAGGAGT GGCTCATACT GTGATTGATG TCAATGGCAT 660
CCCTGGAGTT ATACGGTGCA CATATATCAA GACCACATAT GGTGGCTCTA TCCACTTCCA 720
TGTGGCATTC TTCTTTTTCG CCTTCCCTCA CACCTCACTC AGACCCTCAA GCTAGGATTT 780
ATAACAGTCA AATACCACAG ATACATTTCA GGCCTTGTCA TTGTTGACCA ACACTCGGAT 840
TCCTTGACAG AAGAGACCAC TCCCTCGCCC TTGGATGAGC TCTGGACTCA AACCGCATGG 900
GACAGGATTC CAGCTCTACC ACTCACTAGC ATTGTGGGCG TTGCTGACTT CATTTGGGTA 960
AAATGTGAGT ATCTCAACTG TAGAAATGGT TAAGAATGGT AGCTACTTCA TAGGGTTGTT 1020
AGGAGAGCCA GAGGAAATAG TTTGTAAAGC ACTTAGCACA GTCCCTGATA GATAGAAGGC 1080
ATTCTGGAAA TGCTCACTGA TATTATCTTT TCAAAAATGG AACATAGTTT TCTACAATAA 1140
CACCCTTTCC AGGTTTTGTG ACTCTCTCTT TGCTCTCTTT CCATCTCCTT CACGAATTTC 1200
CATACTACAT CAGACCCTCA AATGTTGACG TTCCCTACAG TGTTCATTCT GGTCTCTTTC 1260
CCCTTCCCTC TTCCCTCCGC TTCCCTCTAT CTCCCTCCTT CCCTTCCCTC TTCTCACTCT 1320
GAGCAGCCTC CACAGCAGTG GCCTCCACTG CCTCCCTGAA GCTGAAGACG TCCACTTTTG 1380
CATCTCAGGC ATCAACTGCT CCAGACTCAA AAATCCCAAC TTCCCATGAG ACCCCTCCAC 1440
TAGGATGTCC TGCTGGAGCT CCCAAGTCAG CACATTGCAA ATGAAAGCAC CACATGTCTA 1500
CTTACTAAGC CTCCTCCCTT CCTGTGTGGT ACCAGCTTCT TCCCGTCGTC CATCCTGGAG 1560
TTTTTCCCGT CACACATCCC CAACATCCAA GTCGTACACA TTCTACCTTC TTAATATTTC 1620
TTGAGTTGAT CACCCACATT TCCATACCCA TTTGGAAAAT CTTACTTCGT TCATTCGTTC 1680
ACAAGTTCTT TCTGGGACCA ATTGCCATCC ATGGTGCCTC CCTACATCCA GGTTCACACC 1740
CTCTAATAAA GTCTGAATAT TAGAGCCTCC CAAACACCAA TCCAGGATCA AATTTTTATT 1800
AATCTGGGGC AAAATGATGA AGAATGCAGT 1830
|
