| Tag | Content |
|---|
EnhancerAtlas ID | HS050-14428 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr11:129697340-129699660 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Sox3 | MA0514.1 | chr11:129699633-129699643 | CCTTTGTTTT | + | 6.02 | | Twist2 | MA0633.1 | chr11:129697401-129697411 | AACATATGGT | - | 6.02 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| 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 | chr11:129697692-129702002 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I129826 | chr11 | 129696789 | 129700444 |
|
Enhancer Sequence | TGTAAGCAGT TATAGCACAG TGGTAAGTAT GTGTGTATCT AAACACGGAA AACATGCATT 60
AAACATATGG TATTATGGCC AGGCGCAGTG GCTCACACCT ATAATCCCAG CACTTTGGGA 120
GGCGGAGGCA GGCAGATCAC GTGAGGTCGG GAGTTTGAGA CCAGCCTGAC CAACATGGAG 180
AAACCCCGCC TCTACTAAAA ATACAAAATT AGCCAGGCGT GGTGGTGCGT GCCTGTAATC 240
CCAGCTACTC GAGAGGCTGA GACAGGAGAA TAGCTTGAAC TGGGAGGCGG AGGTTGCCAT 300
GAGCTGAGAC TGCACCATTG CACTCTAGCC TGGGCAACAA GAGCGAAACT CTGCCTCAGA 360
AATAAAATAA AATAATTAGC CGAGCGTGGT GGTGCACACC TGTGGTCCCA GCTACTCAGG 420
AAGCTGAGGC AGGAGGATCA CTTGAACCCT GGGGGCGGAG GTTGCAGTGA GTTGAGATCG 480
TGCCACCGCC CTCCAGCCTG GGCAATAGAG TGAGACCTTG TCTCAAAAAA AAGAAACAAA 540
AAAGTATTAT AATCTTATGG GGCCACCATC ATACATGCCG TCTGTCATTA ACCAAAATGT 600
CATTATGCGG CACCTGACTG TATACAGCTG TCTACTAGAT TATAAACTCC TTGCAGATAA 660
AACTATTCAT TTCATCATTA TCCATTGTAT TATTTCCTTA GCACCCAGAA GAATCCTGTA 720
TTTAATTGGC TCATATGGAA AATTTTAGAA AGAGAGAGAC AGCAGGGCTG AGACTATCTT 780
CTGCTCAGGA ACCAAAACGA GCTGGGAGGT AACAGAATTC TTTTTCATAG TAATTGTATT 840
CCATATCATG GTGAAATCGT GCCAGAACAA GCTTCAGACT CTTTCTGGTC TTACTCCTTC 900
TGACCGTGCT GTTCCCAAGA ACCTCCCACA CAGGAAATAA CAATGATGGC AGTAGCTGTC 960
AAATTCTAAA GACGGGGATA GACTCTGGAC CTCCTCAGGC CCCTGAGCCC ACTGTAGAGC 1020
AGGGACGTGA CTTAGTTGAA GTTCAGGACT GCGGCCACAG TCACACCACC TGTAAGCAAT 1080
GGAGGACTTT CAACACAGAA CTCTCTGCTT CCCCTGCATT CTGTTACTAA GCAGCTCATA 1140
GAACGTGAAG AGGTATTAAC CTTGTTATTT GCAGAGTTAC AAAAAGCTGA GTCAGGTAGG 1200
TTTGGCTGTA TTCCAAAGCA AACCCAGACC AGAAGCCACC TGAGAGTTCC TGCCGGCAAG 1260
GACAAATTCA GAATGTAGAA AAACGATGAA AATAAATATT CTATGATCAC CCTATAACCT 1320
ACTTCCTTAC TGACCAAACA CACGTCTCAT TCCCATTAAC AAGTTATGCT CAGCCACTGC 1380
CCTCTCTAGG ATTATGTGAT GTTAAACAGT AATTCTGCCC ATTTAGGGTC AGCTACTCAA 1440
AAGCAAAGAA CAGCAACTTT AGGTCAAAAT ATGTTCTTCT AGGAGAGAAG CCTAAGTCTC 1500
TCCCCTATTA TTGCACGAAT AGTGTACCAG CACCAGACTA GAGAGGAAGT TAACACTTAT 1560
TAAACATGTA TTCTAGTCAC CTGCTAGACA TTTTCAGGTA AGCCTCACAG GATCCCTCCA 1620
AGGTGGTATT AATGTCCCTG TTTTAGAAGG AGGAGTACTG AGATTCACAG ACATTAGAGA 1680
ACTTGTCCAA GGTCTTACCA GTAAAAGTGG CAAAACCAGG ACTGAACTTA GGTCTGACAC 1740
TACATAGTTC ATATTCTATT ATGTGACTAT ATTCCTCCTT AAAGGAAAAT TTAGGAATTC 1800
AGTTTCCTTT AGGAAGATGT AGGAAATAGA ATGTACTAAA ACTAAGATAA CAGTTGACTT 1860
AAGTCTTTTC TAACTCAGCC TTCCTCAGGC CCATGTGTGA GTTGGTTTCT ATCCTTTCCC 1920
TGAAACTCTT GGGCACATAG GAACATAATG TCTGTTTGAT TTTACTTTTA AGTATATTCT 1980
TTTGGTCAGT CCCAATCTGA CAAAATTTTA AGATTTAATG CATTCTATCC ATGCAAGAGA 2040
ATTACATGTG GTTTTGCTTG TAAAGAAGGT GGGAATGATA TAGGGTAAAG AGAGTAAGTG 2100
ACATTATCTA GTTCACTCCC ACCATATGGA TGATTGGCTG CAAGTGCCTC TCAGCCTTTG 2160
CATGTGTTAT TTGCTCTGAC TAGAACTCTG CCCACACTAC CTGACTAATG CCTGTGTGTT 2220
TTTCCAGGAA GCTTTCATGA CACTACCCTC TATAATCTTT CTCCTGTTTC CTCCAGGCTG 2280
AATAGGAATC CTCCCTTTGT TTTCATTGTT ATTAGTGTTC 2320
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