| Tag | Content |
|---|
EnhancerAtlas ID | HS176-11872 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr13:99427040-99428900 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr13:99428796-99428811 | GAGGTCAGAAGTTCA | + | 6.38 | | RARA | MA0729.1 | chr13:99428796-99428814 | GAGGTCAGAAGTTCAAGA | + | 6.88 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27651 | chr13:99427477-99429705 | Fetal_Intestine | | SE_28565 | chr13:99427274-99429851 | Fetal_Intestine_Large |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I098775 | chr13 | 99427743 | 99429621 |
|
Enhancer Sequence | TCCCCACACA GCCGGCTTGG GAGCCAGGTG GCCATTTTCC CATGTGAAGG AGAATATTTC 60
CCTCCTCATT CAGGGCATCT GGGGTTGGGG GCCAGGACCT CCTCTGTCCC TGCTTCTCCT 120
ACATCCATCT GTCCAATGGA TGCCAAGCTT CGACTGGTTG CCAGGCATGG GGCTGGGCCC 180
CAGGAGAACC GGAGCAAGGA CGAGACCTCT TCTCCATCCT GGTGAAGCTC TGTTCCTGGG 240
CGGGTTAGTC AGGTACTCAG GACACCACAG AGGGCAGTGG GTGGAGGGCT TCAAAGTCAT 300
GCCCTCGGTA ACTGGCCAGC AAGTGTTGCC ACCAAGAGCC GTAAGGGGGC TTCAAAACGC 360
TGGCACCTGC TACTGAAAGG TTTGTGGAAT CTTCTTGAGA TTAAAAATGA AAATGCTGCT 420
GGCCTCTGTC TCTACACATT CTCTAGTGAC TCTGTGTCTT CATCAGGGCA AATCATTCCT 480
TGCAATAAAT ATCTTGAAGG TGTTCAATGA GCTGGCTAGT TAGAGCTTCT CTGGAGCCCT 540
GTGTTCGAGT GGGACACTTG ACTTTTGCTG TCAGGCCCCT CTTGGCATTG GGGTCACAGG 600
GAGCAGTGAT TCTCACACCC TACTGTGCAA AGGAATCCCC TGGGGCTTGT TGGAATGCAG 660
ACTTGCGCTC GGTGGCTCTG GGTGTGGACG AGGACCCTCT GCCCGCAAGC TCCCAAGTAC 720
TTGTCTGTTC GCGGCTGCTG GGCTGCAGGT CACCCCTTGA CCAACAAGAG CTTAGACGGA 780
GGCTTCTCCG CCGTGGCTGT ACTGCTGTCC TGGACGATCT CTGTCTGTTG TGGGGGCTGT 840
CCCGTGCACT GTGACATGTT CAGCAGCATC CCAGCCCTCC ACCCACAGGG TTACAGTAGC 900
ACCCCCACCC TCAACCATGA CAACCAAAAA TGTCCGCAGA CGTTTTCGTT TGCATCCCCT 960
GGTGGACTGG GGCATGGGGG CGGGGTGTTG AGAACCACCG ATTAGTAGAC TTTCAAAGAC 1020
TCTCCCAAAT CCAGTTTTTT TGTGATCAAA AGTCCACATC AAATCCTCTT AGTTGGAAAA 1080
CACGCATCAC TCTAAGGCTG AAAAAGATGA CTCCACAGCT GAGCTCTAAA TGTCCTCTTA 1140
AAAATATAAA ATCCCAGATC AACCTGTCTT CACAATGGCC GCATGTAGCA GCCCCTCCAC 1200
AAAGACTGGG TACAGTGGCA TTTGCACCTT CTAAGGGACC CTGGAGTGCG GCCTGACTGA 1260
GAGAGTGGAT GGGGAGGGGA TGCCGGGTCT CTGGCTCAGG TGTTGCGTGT TGGGAGCCCA 1320
CTAGGTAGAA CAAGTGTCCT CCACCCAGCT CAGCTCCGGA GCCTTCCTCG AAAGGCAAGA 1380
GGTCAATTCA TCTTCTGCCT CAGCAGAATC GTCCCTTCCT TTACAAGGGG ACTTTGCTCC 1440
ATGATCTGAC AGACCTGGGA AGTGTGTGGA GGTTTTACAC GATGACTCAG TGCACATCAG 1500
AGTCAGAGAC AGGACGGCCG AACACTGATT CCAGAGATAG GCATGTGGGC CCCGCCCGGG 1560
AAGGAGAGCT GCCTGGGAGA TGGGGAGCTG CAAGAGAGCA CCCAGAGGGG TAAATTTGCA 1620
CAAGGCCACT GCGTACACTG GTACGTGCTT CCTTGAAAAT GTGACATTTT CAGGCAGGGC 1680
GCGGTGGCTC AAGGCCGGGC ACGGTGGCTC ACGCCTATAA TCCCAGCACT TTGGGAGGCC 1740
AAGGCGGATG GATCACGAGG TCAGAAGTTC AAGACCAGCC TGGCCAACAT GGTGAAACCC 1800
CATCTCTACT AAAAATACAA AAATTAGCGG GGCGTGGTGG TGCATGCCTG TAATCCCAGC 1860
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