| Tag | Content |
|---|
EnhancerAtlas ID | HS133-02124 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:117013940-117016040 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GFI1 | MA0038.2 | chr1:117015458-117015470 | CAAATCACTGCA | + | 7.22 | | Hnf4a | MA0114.3 | chr1:117015191-117015207 | GAGGGCAAAGTCCTGT | + | 6.07 | | Nkx2-5(var.2) | MA0503.1 | chr1:117015396-117015407 | CTTGAGTGCCT | - | 6.14 | | RREB1 | MA0073.1 | chr1:117014694-117014714 | CCCCCCACCACCCCCCATCC | + | 7.75 | | SPIC | MA0687.1 | chr1:117015285-117015299 | AAAAAGAGTAAGTA | + | 6.52 | | Stat6 | MA0520.1 | chr1:117014435-117014450 | CCCTTCCTCAGAAGT | + | 6.01 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_27848 | chr1:117013898-117021408 | Fetal_Intestine | | SE_28774 | chr1:117013873-117021547 | Fetal_Intestine_Large | | SE_50584 | chr1:117013866-117016332 | Sigmoid_Colon | | SE_52493 | chr1:117013950-117016256 | Small_Intestine |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I116471 | chr1 | 117014027 | 117021401 |
|
Enhancer Sequence | TTGATTGCTG AGTTTTTTCA CTCTGCCCCC ACAGCTCCCG GACCTGGGGG CCCCCACCCC 60
GTGAGCTCTG CCTTCCTGAT ACACAGATTA CAGGGGAAAC TCAGACTCCC TCTGCAGGAG 120
CTGGATGTCA GTTATCACCA GGGCTCAGCT GCGTATCCCG AGGGCTCACT CTGCTTGCCT 180
GATTCACCTC CCTTTCCAGT TTTGCCTTCC CTTCTTCCTC TAGCAGTCTG AGCATTCTGC 240
ACCTCCCCCT CCCTGTGCTT CAATGCCATC TCACCCAACA TCCACACTAG GGCTGCATGT 300
TCTCCAGAGC CTGCTCCATC CTTCCCTTCC CTTCTACCCA CAACTGACTT GCTTTATAAT 360
GGAAGAAGCG TTTTAATGCC TGCCATGAAA TCCTGTCATC TGGACAGGAA GGGCAAGCTC 420
CCTGGCTGAA TCATCAAGAG GAGAGCACCT GCCTGGAATA AGGCTCTGAA TCTTCTACAG 480
CTCTCTTTTC TGTTTCCCTT CCTCAGAAGT ATCCCCTGGA CACCGCAGAG GCTGTAGAAC 540
CAATACTGCC TGCACTGGCC AACTGTGGGG GCAGTGGCTT CACACCCCGT GTGTGCTGCA 600
AACACACTCA AATCTATGGC CTGTAATAAT TTCTGCACAT CCCTGTGTTG CTCCCATAGG 660
ACAGATAGAG GCACAAAGGC CCTGGCTGAT AAGTCGCATC AACTGATCAC ATAACCACTC 720
ATTGACAAAA CAGAGATTAA ACCTATATTT TTGACCCCCC ACCACCCCCC ATCCTGTGTC 780
CATTTCATTA TTCCATAAAC ATTCCCCTCT ACCACACCCT ACTTCCCCCT CACCTGCCCA 840
CCCCTGCAAA GTCACTTGAT CTCTTGGTGA ATTAGCATGA GCCAACATTG ATGTTTTAAA 900
ATAGCAAATT TTCAGGCTGA AAAAAGTCAA GATCATCTTT AAGTCCCCAA GGACATATGC 960
AACCAGTGAT AGAAAAATCC TCTCCCACTT CTCCCCCTCC AGTCTGAATT GACTTAGCAA 1020
CTTTTCTTCA GCTCCTCAGC AGAGCCTTTC ACAAATTCCC ACTTGCAGCA CTGCTGAAGG 1080
ATAGACATCC TGATGTGCTC TCAGCTGGAC TGCTGCTGTG GGCTTCAAAA AAACAGATGC 1140
AGCAGCAGTG AGTGTGTGCC TGTATTATAT TTCTCAAGTG AACATCTTCA GAAGCTGGGG 1200
ACATGTGTTT TCTAGCCCAG CATGTAGGAT CTGTGGCCCC TGAGGCTGTG GGAGGGCAAA 1260
GTCCTGTAGA GAAGCTATTG TTTTCCTTGC CTTTGCTGAT AGCATGAGAT CAGCTAAATG 1320
ATGGTGGCAG GTATCCAAGA CCAAGAAAAA GAGTAAGTAG GGGTACAGTA ATGGGAAGCA 1380
GTAAATCGTA GGACATATTT GTAATCTAAG CAACAAAAAT CAAGCATTCT CTGGGAAATG 1440
CATGAAGCAC TGAATGCTTG AGTGCCTAAT GGGTTTTGAA GCCTCAGTAA GTTTATGTGG 1500
ATGGGTGCCA AGAGCAAACA AATCACTGCA GCCACAAGCT GCCTCACTCC ATATCCGAGA 1560
TGCATACTGA GAATGACTGG GAAGGCTACT TGGTATGGGA ACCCTAAAGC AGTTAGGATG 1620
GGGAGGCCCC CGGGGAAATG CTATCCTTAG TGCTCTCCAG GAAGCATCAT TTACAACTTC 1680
ACCATTGGCC AAACACTAAT ATATGTGCTT TACATATATC ATCTCATCGA AGCCTCATTA 1740
TAACACTAAT GGGTTAGGTG TTATTACACC CCTATTTTAA AGATGAAGGA AGTCAGACTC 1800
AGTTAAGATC ATACATCTAT TAAGAGGTAG GGCAAAATCC AGACTCAGTC TTTTCTGATT 1860
CCAAAGCACC TGCTCTTAAC TGCCCCACTT TATTGCCCTC AGAGCTCTTT GGTACCAATT 1920
ACACCAGGCA TTCCTAGCTA CAAGGCATTG TTCATTCATT CATCCATTCA TTCAACATCC 1980
AGCAATATTT CTTGAGCATC TGCATCGTGC CAGGCCCTTT GCTAGGCCCT GGGACCTCAC 2040
TGATGAAGGA GACATGGACC CTGTCCTCAT GGAACTTGGA ATCTAATGAG TGAGTGCCAG 2100
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