| Tag | Content |
|---|
EnhancerAtlas ID | HS133-03632 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:224254820-224256380 |
Target genes | | Number: 14 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ALX3 | MA0634.1 | chr1:224255855-224255865 | TTTAATTAGA | - | 6.02 | | Nr5a2 | MA0505.1 | chr1:224256123-224256138 | CCTGTCCTTGACCTC | - | 6.16 | | Stat6 | MA0520.1 | chr1:224255030-224255045 | GTTTTCCTGAGAATC | + | 6.03 | | TCF3 | MA0522.2 | chr1:224256157-224256167 | AACACCTGCT | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 224255307 | 224255780 | | chr1 | 224256099 | 224256324 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I224067 | chr1 | 224254881 | 224256038 |
|
Enhancer Sequence | CAGACTTCCA AAGTGCTGGG ATTACAGGCG TGAGCCACTG CACCCGGCCT CCCTTTAAGA 60
ATTAATTTCC CTATTGAATC ATTTAAAACA AAAAAGGCTC TGTAGATTAT CACTGGGTTT 120
AATCCTGTCT AGAAGCAAGA AACACCAGGG TGAATTTAGC TAAGACCCAA TTCTTAAGTA 180
CTTGCCTAAA TGTCTAGGAT AGTTATGAGT GTTTTCCTGA GAATCTTCAA GGAAAGAAAT 240
TCAGTTTCCT GAAATAGTTC AGGCTTCAAG TAAAACTGCT ACATAGGAGA GTTAAATTAA 300
ATAACCTCTA AAAGTTTTTT TCCAACCATG GCTTTCATTT TTAATTGTCT TATGCTTCCC 360
CCTCTCTCTC ATTTCAAAGG TAATCAGGAA GTCTCCTAGG ATAAGGTTAT TATATTCAAG 420
TCCTGCCAAA AAATGTAAGA AAAGAAGCTC CTATTTGAGT GGACCAAAAA GAACAATTAT 480
ACCTCCTAAA AATAAAATGA ACCTAAGCTA AGAAAATGAA AAGGTTTCTA AAGAAGGTCA 540
GTACTTCTTT TTTGGTCTCC TTTCATCACT GTGTGATTTA CTTTAATAGT ACCCTGTCAA 600
ACTAGATGAC TCAGTGGCCT CATCACAGCT TACAGAGCAT TTCATCTGTG GTCATTCATC 660
CTGCCTATGA AGAAATTGAC ATGTAGTCAC TACAGAGCAA CACTGCTCAC CAATGGTTGT 720
TCACCACCAT ACCCTCCTGA TCCTTGCCTA ATCAAACAGA GAGATGCTAT CCTGCTTTTA 780
CCTACACAGA AAAAGAAAGA AGATAAAACA ATGTTAGGGG GTTGTGGCTC ATTGATGGTC 840
AGATATGAAA AGCTGCTTCA AATGCTGTCC CATCAGTTCC TAAAACTGCA ACATGAAAAT 900
GCATCATCAT GACTACCCTT TACCTATCTC CCAAGCGTGA AATTGTTTTC CCCAGTAAAA 960
GTTTAAGGAA ATGAAGTAAT TGCTGTTTGG GGCAGGAATG CTATGAGTAT TACCATGCAG 1020
TTTTTTCCTT AAATGTTTAA TTAGAAGGAA GTATGGCATT CTTACAGCTA TTTTTTAATT 1080
AAGCCAGCAG ACTCTACCAA GAATCTGATC CCCTCTCTAA GCAGATAATT ACAGTGACAA 1140
GTGACTTTCA AGTTTATGCC CATATATACT CCTAGACTTC TGATGTGCCC CAGAAGGACG 1200
TTACCATTCA TGTTCTGAGT GCTGGCCTCT GGGCCTGACC CTGTCTGCCT GGATTTGGAA 1260
CTTTGCCTTT CCTTAACTTG TGACTTGCCC CCCTAGATTC CAGCCTGTCC TTGACCTCTG 1320
GCAACAGCAA ACTCGTTAAC ACCTGCTCCG CATGCATAAA TCCTTGCCTT CTGCCCAATT 1380
CTTAATTCTG ATTTTTGGAC TTCTGGACCA GGCTAATCCT TACAGTCTGG GGAGAATGAA 1440
AACATTGTTA GACTGAAATA GCTAAGCCCA GAGTTTATGA TTAATGAGGA CAGACAGGCC 1500
AAGGAGTCAG TAACCATACA AATGTTCACA AATGATTTGC CATAAGGCCT TAGATTTTAC 1560
|
