| Tag | Content |
|---|
EnhancerAtlas ID | HS133-18089 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr2:219587190-219588500 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HOXA13 | MA0650.2 | chr2:219588058-219588069 | GTTTTATTGGG | - | 6.62 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_04466 | chr2:219586997-219588657 | Brain_Anterior_Caudate | | SE_05726 | chr2:219587151-219588735 | Brain_Cingulate_Gyrus | | SE_07667 | chr2:219587076-219588726 | Brain_Hippocampus_Middle_150 | | SE_09430 | chr2:219586939-219588899 | CD14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr2 | 219587269 | 219587387 | | chr2 | 219587773 | 219588200 | | chr2 | 219587834 | 219588207 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I218722 | chr2 | 219587524 | 219588123 |
|
Enhancer Sequence | GTAGGACAAT ATTAGATAGG ATTGACAAGG AAGGCCTTTT TAGTTGAATA CTGAGTGAAA 60
GAACTAAGCC AGCCATTCAA AGATCTGAGT GTTTCAGAGG AAACCACAAA GATCCAGAGG 120
TGGGAACGTT CCTCATGAGA GGAAGAGTGG CTCTGGATAA GGTCAGAGAG TCAGGAATCA 180
GATCACATAG TCCTGGAAGC CATCAGATGA TCTTAAGCTG TGTTTTAAAA AGAGTACTGT 240
GTTTTGAAAA AGTAGCCACT GTCTGGAAAA TAGATGATAT AGAAGCCAGT AAATCAGCAG 300
TTGAGAGATG ATGGTAGCTT GACTAAGGTA ATGACAGTGG AAATGGGGAA GAATAGCCAG 360
ATTCAAAGAC ATATATTTGA AGCTGGAAGG ACTTGTTGAT GGATTAAGTG GAATTGAAGA 420
TCTGCTGAGG TCAGGGTGAA AGCATCATTA TGACAGGCAT GTCGGGAGTT TCTGTGTTGT 480
ATGGAGGCCT GTCCAGGGAC TAAGCTCCTT CTGCCTGAAT ATTTTTTATT GAAGTCTTCT 540
TTGTGCAATT ACAGCTTATT TCTTGGCCCT GACTCTGAAA GATTAATTGG ACAAGAGGGG 600
AATGTGATTG ATCTGTTCTT CTCTCACTTT CCCCTAGCAT GACTTGGTTA GAATCTGACA 660
TTCCCACCTT ACTTTCAAGG AGATTAACAG ATAACATGTT CTTTTCTTTT GAATAACAGT 720
GGTTATAGAA CCCTTGAGCT TGCCACAGTG CCCTCCTTGT TTCTTTGACT CTAGCCCTAA 780
AATCCTTATC TCAGCCTCTA GGTTCCTGTT TCTCAGCTGG GTGCTGACAG CAACTGTTTT 840
CTCAGTTGAG GGCACAACAA GGACTTGTGT TTTATTGGGA TGTGAGGTTT TACACAGAAT 900
CACATTTAAA TAGCATTTTC CCTCTAAGTA TTGGAGACCT CCTACCAGCT TGTATGTTGA 960
TGGGTCCTAG AGAAAGTGCT TCCATTAAAC TTTATCTGCC AGGCTTGAGT AATATGCCTT 1020
CCCTTGAACT CCCCTTGAGC CAGAGTTTAC AAATTCACTG GCCATTGAGA GAGGTTGATT 1080
AATGGGTGCA AATACACATT CAAGATGATG CATTTTTGTT TGGAAATTGC AGAAGTGATG 1140
ATATATCCTT AAGTGCATCA TATCATGAAG CACATAATAT CATCATTAGT AATAGTACAA 1200
ATTGACATGG GCCTCATCAT AAGATGCAAC TAAGGATATA TCATCACTTC AGACAAGGCC 1260
AAATTGAGTT TCATTCTTTA GAATAACTGG TCTGTATTCT TCAGAAGTGT 1310
|
