| Tag | Content |
|---|
EnhancerAtlas ID | HS133-07742 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr12:67819860-67822360 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PBX1 | MA0070.1 | chr12:67820938-67820950 | ATTGATTGATGG | - | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_29364 | chr12:67818078-67830642 | Fetal_Intestine_Large |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I067424 | chr12 | 67818453 | 67826617 |
|
Enhancer Sequence | GCCCTGATCT TGTACACAAT TACCTGTGAT AAGAGCCATG TGTGAGAGTT CCACCTGAGT 60
GGAGACTAAA TGGCACGCTG CTGGAGTACT GAGCAGAGAG GAATCACATG ACTGTGAGCT 120
CAGATCATTT CTGGGTAGTC TCAAACCTTT GGCTGAGTGC CTAAATCTTC ATTTCACCTC 180
TTGCTGTGAA ACTCTTGTTT TTCTTTAAAC CCAAGAGTCC AACTCCATGT GTAATACAAT 240
ATCATGTAAA TGAGGGTAAC CTTGGAAGGC AGGCTGCTTG TCATACTATA GTGGCTTTGT 300
TGCTGTAATG AAAACCACAT GCTTCATGGT ACTTTTAGAC TAGTTAATAT TAGCAGATCA 360
GCTGCATTTT TGTTTAGATA TTGCTATTCC AGCTGTGCTT TTTCTGGTTA TTTCAAGAGA 420
ATTCACAATT TCTACCAAGC CATAAGCTTT TTTCAGGAGA GTGGAGAACT GGAAGAAAAT 480
GGCCAGCACT TTCCTCTCGG CTCTCTGGTT TCCACATGGA ATTTGTCATT GTTTTCCCGA 540
GTCATTGTGA AAGGAAGACG TGGTTGACCC AGGGACTTGC TTTCAAAGAG TAATGGAATA 600
AATAGCAAGG TGAAAAAAGT ATGAAAAATG ACTTGACTTT GTCCTGGGGC GAAGAGAAAA 660
GAGTAGAAAA TAAGAAAGAG GGAGGAAAAG GGGCATGCCT AACCACCTTG CTGAGATCTT 720
GAAATTTGCT GGAATGATAT GGTTATGATT ACGATTATGA TTATGAGTGT TTTGAGAAAG 780
GGAGGATCAT TTCTTTCCAT TCTTGAGTCC TCTTTGGAGT CATTTGAATC TCTAAATTTG 840
CTTCTCAGAG AAAGTTTTAT ATTTCTTGGG GAAGATCTTA AATTACTTTC TTTCCCAACT 900
AAATTGGGTC CCTCTTTCTC TACCCAACAT TAAATATCCA ATGTCCCTGT GACTGGAAGA 960
GTCCCTTCTC TCTCTGTAGA AAGAAACTGG GGCAGACAGA GAACTTTGCC TCCCAATCTA 1020
GTAATGTCAT TAAGAGCAGT GATCTCAATC CTTAGGGTAG ATCTCTGTGG ACCTAAAGAT 1080
TGATTGATGG GCACTTTCTC CTCTGCCCAG CAGGCTGGAG GAAAAGGGGT ATAAGAAAGA 1140
AACTTTCAGA GTTCCTCATA ACAATCTTAA GGGCAAAGAC CTGTCTGCTG AGGATTAGGT 1200
TAGTTTGTAC CATACTCACA GAATCAGCAG CTCAGACCCC TCTGTCGGTG GGGGATGGGG 1260
CTGATGAGAT TTTGCTTTGG CATGTGTGTT GCTTAACCAA TGTATTGTGC ATATATTGAG 1320
CCCAATAGCT ATGAACAGGA AACTACTTCA TTTTCTCTGC CATGACAACC TTGGAAATAT 1380
ACTGTGCTCA ACCTTCCCTC CCTGTCTGCG TCTGTAGTCT GATCATGTTC AAGCAACAAA 1440
AATGAGTCTT TTATTGAGGA TTATGACTCA TCTATAAGTA CGAAAAGACC CAATAGAGTC 1500
TAAATCAAAG CCTTTGTCTC TTCACATCTT CTCTCATTTT CACAGCCCGG GCCTGACCCT 1560
TGCTGGGGTT CCCAAAATAG GAAAGGAGAG TCTGGTCTCA TGGTCTGTTT TTTCACTTGT 1620
TCCTGACTCA CTCCTCCTCC CCGATTTGCC TTGCTGCTTT TGGTTTCTCC ATGGTAGGGG 1680
AGTGGGGCAG AAAGGGAAAC AGAAGATGGG CAGCCTTTTT AAAGTATCTG GTGCTCTTTG 1740
TGGCTCTGTC TTGGCTGGCT TTGCCCAGAT GCTGGGCCCT TCATTACACT TTTCCATGAT 1800
GTGCATTTGT GGATCCTATG CATTGGGACT TTTCTGATGT ACTAGTTTAC TGCTATTGGT 1860
GCATGCTCTT CAGCCGACCC CATGCGTCCC ACTTTCCTTC TTCCACCCCA ACTCCTGTCT 1920
TAGCGGTTGT ACTCCAGCTT CTCACTGCTA ATATCTCCTT GCTCTGGCAG GCCACCCTAT 1980
AAGGTGGGCT CCTTTCAAGA TGTTTCAGGA TAGATTCCAT GGTGTCCACC AGGCTTGCAG 2040
GAACCCCTGC ATTCCTGCTC TACCCCACCA AGGAAAATAA GGCTGCTTCC CCTGCTGCCT 2100
CTGTCCTCGC CTGCCCTCTT GGCAGTTCTT GGCAGGTTCC TGACCTCAGA AATTGTCTCA 2160
ACATGAGGCA GGCTGTGGTC TCTGTTCAAC TATGTCCTCA AGTCTTCAAG GACACATGTC 2220
AAGTTCTCCA GTGGGAGAGA AAAGCCAAGG GATCTCGATT CTCAGGCATT CCCTTCAACG 2280
AGCTCTCTTG GGGACTTTCA AGTCTTCCTT TACATACTCT GGAGGTGAAA GATCAGTTTG 2340
GGCACCTTCT AGTGAGCCCT GGGATCCAGC AGGTCTCTGT AGGATTGGGG ATAGAGGTGC 2400
TTGCTACTTA TTGTTTTCAC TTTAGGGGCT TCAGCCAAAA TGCAGAGAGA GCAGGAAAAT 2460
CCCATTTGCA CCTAATGAAA ATGTGTAGGT TGAAAGTTCA 2500
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