| Tag | Content |
|---|
EnhancerAtlas ID | HS118-04052 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr11:129697020-129699240 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Twist2 | MA0633.1 | chr11:129697401-129697411 | AACATATGGT | - | 6.02 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_27353 | chr11:129696704-129697487 | Esophagus | | SE_27353 | chr11:129697541-129700314 | Esophagus | | SE_27846 | chr11:129697695-129699850 | Fetal_Intestine | | SE_28695 | chr11:129697699-129699937 | Fetal_Intestine_Large | | SE_35121 | chr11:129697671-129700326 | HeLa | | SE_36539 | chr11:129697544-129701852 | HMEC | | SE_64293 | chr11:129696762-129697554 | NHEK | | SE_64293 | chr11:129697692-129702002 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I129826 | chr11 | 129696789 | 129700444 |
|
Enhancer Sequence | CCACTTTGTG TGCTATGTGC TAGGACTGCT ACCAGTACGT CCCAGGACAA TCAGTCTTTC 60
ACAAGTATTG TCATGTGGTG CTTAACGACA GGGACATGTT CTGAGAAATG TGTCGTTAGG 120
CGATTTTGTT GTGTGGACAT CCTAGAGTGT ACTTACACAA ACCCAGATGG CATAGCCTAC 180
TACACATCTA GGCTATGCGG TGTATACTGT CAGTGCTGAG TATACGCACT GTTAGCAGAT 240
GCTGAAGGGA GTCTGTAGGT GTGAGCACTT TTTCCAAGAA CTGACTTCAA ACCTGTACAG 300
CACATTACCG TACCACACAC TGTAAGCAGT TATAGCACAG TGGTAAGTAT GTGTGTATCT 360
AAACACGGAA AACATGCATT AAACATATGG TATTATGGCC AGGCGCAGTG GCTCACACCT 420
ATAATCCCAG CACTTTGGGA GGCGGAGGCA GGCAGATCAC GTGAGGTCGG GAGTTTGAGA 480
CCAGCCTGAC CAACATGGAG AAACCCCGCC TCTACTAAAA ATACAAAATT AGCCAGGCGT 540
GGTGGTGCGT GCCTGTAATC CCAGCTACTC GAGAGGCTGA GACAGGAGAA TAGCTTGAAC 600
TGGGAGGCGG AGGTTGCCAT GAGCTGAGAC TGCACCATTG CACTCTAGCC TGGGCAACAA 660
GAGCGAAACT CTGCCTCAGA AATAAAATAA AATAATTAGC CGAGCGTGGT GGTGCACACC 720
TGTGGTCCCA GCTACTCAGG AAGCTGAGGC AGGAGGATCA CTTGAACCCT GGGGGCGGAG 780
GTTGCAGTGA GTTGAGATCG TGCCACCGCC CTCCAGCCTG GGCAATAGAG TGAGACCTTG 840
TCTCAAAAAA AAGAAACAAA AAAGTATTAT AATCTTATGG GGCCACCATC ATACATGCCG 900
TCTGTCATTA ACCAAAATGT CATTATGCGG CACCTGACTG TATACAGCTG TCTACTAGAT 960
TATAAACTCC TTGCAGATAA AACTATTCAT TTCATCATTA TCCATTGTAT TATTTCCTTA 1020
GCACCCAGAA GAATCCTGTA TTTAATTGGC TCATATGGAA AATTTTAGAA AGAGAGAGAC 1080
AGCAGGGCTG AGACTATCTT CTGCTCAGGA ACCAAAACGA GCTGGGAGGT AACAGAATTC 1140
TTTTTCATAG TAATTGTATT CCATATCATG GTGAAATCGT GCCAGAACAA GCTTCAGACT 1200
CTTTCTGGTC TTACTCCTTC TGACCGTGCT GTTCCCAAGA ACCTCCCACA CAGGAAATAA 1260
CAATGATGGC AGTAGCTGTC AAATTCTAAA GACGGGGATA GACTCTGGAC CTCCTCAGGC 1320
CCCTGAGCCC ACTGTAGAGC AGGGACGTGA CTTAGTTGAA GTTCAGGACT GCGGCCACAG 1380
TCACACCACC TGTAAGCAAT GGAGGACTTT CAACACAGAA CTCTCTGCTT CCCCTGCATT 1440
CTGTTACTAA GCAGCTCATA GAACGTGAAG AGGTATTAAC CTTGTTATTT GCAGAGTTAC 1500
AAAAAGCTGA GTCAGGTAGG TTTGGCTGTA TTCCAAAGCA AACCCAGACC AGAAGCCACC 1560
TGAGAGTTCC TGCCGGCAAG GACAAATTCA GAATGTAGAA AAACGATGAA AATAAATATT 1620
CTATGATCAC CCTATAACCT ACTTCCTTAC TGACCAAACA CACGTCTCAT TCCCATTAAC 1680
AAGTTATGCT CAGCCACTGC CCTCTCTAGG ATTATGTGAT GTTAAACAGT AATTCTGCCC 1740
ATTTAGGGTC AGCTACTCAA AAGCAAAGAA CAGCAACTTT AGGTCAAAAT ATGTTCTTCT 1800
AGGAGAGAAG CCTAAGTCTC TCCCCTATTA TTGCACGAAT AGTGTACCAG CACCAGACTA 1860
GAGAGGAAGT TAACACTTAT TAAACATGTA TTCTAGTCAC CTGCTAGACA TTTTCAGGTA 1920
AGCCTCACAG GATCCCTCCA AGGTGGTATT AATGTCCCTG TTTTAGAAGG AGGAGTACTG 1980
AGATTCACAG ACATTAGAGA ACTTGTCCAA GGTCTTACCA GTAAAAGTGG CAAAACCAGG 2040
ACTGAACTTA GGTCTGACAC TACATAGTTC ATATTCTATT ATGTGACTAT ATTCCTCCTT 2100
AAAGGAAAAT TTAGGAATTC AGTTTCCTTT AGGAAGATGT AGGAAATAGA ATGTACTAAA 2160
ACTAAGATAA CAGTTGACTT AAGTCTTTTC TAACTCAGCC TTCCTCAGGC CCATGTGTGA 2220
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