| Tag | Content |
|---|
EnhancerAtlas ID | HS061-04123 |
Organism | Homo sapiens |
Tissue/cell | GM12892 |
Coordinate | chr11:60916050-60917950 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr11:60916754-60916770 | CTCAAAGTAAACAAAC | + | 6.28 | | FOXC1 | MA0032.2 | chr11:60917234-60917245 | ATATTTACATA | - | 6.62 | | FOXP2 | MA0593.1 | chr11:60916758-60916769 | AAGTAAACAAA | + | 6.62 | | Foxd3 | MA0041.1 | chr11:60916762-60916774 | AAACAAACAAAC | - | 6.32 | | RREB1 | MA0073.1 | chr11:60916398-60916418 | GGGTTGGGGCTGGGTTGGGG | - | 7.57 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_09422 | chr11:60916713-60918248 | CD14 | | SE_29266 | chr11:60916582-60922165 | Fetal_Intestine_Large | | SE_31646 | chr11:60913799-60921667 | Gastric | | SE_42023 | chr11:60916861-60917210 | LNCaP | | SE_42023 | chr11:60917258-60918987 | LNCaP | | SE_65694 | chr11:60912444-60919190 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I061148 | chr11 | 60915634 | 60921982 |
|
Enhancer Sequence | AAAAAAAAAA AAAAAAAAAT CAAATCATCA AGTTCTTCTC ACCTGATCCA AAGCAGCACT 60
GAACTGACTT TCCCCACAAG TGGAAAAGTT ACAGTGTAAA CCATGGAGAG GAAGGCGTTT 120
TTAGTTTTCA TTTTTTTGCG TTTTTAGTTT TCTTTTTTTT CTTTTAAGAG ATGAAGGACT 180
CGCTCTGTCA CTCTGTTGCC CAGGCTAGAG TGCAGGGACG CAAAAGTAGC TCACTTCACA 240
GCCTCAAACT CTTGGGCTCA AGCAATCCAC CTCACTTCCC AAGTAGCTGG GAGTCCAGGC 300
CTGTGCCACT GCCCCCAGAT GGCTTTCATC CTTTCTAAGG AATTGCTGGG GTTGGGGCTG 360
GGTTGGGGTT GGAGATTCCT CCCACCCACC AGGGATAAAT AGTTAAGACT ACGTGAAGAG 420
GGGCCAGGCG CGGTGGCTCA CGCCTGTAAT CCCAGCACTT TGGGAGGCCA AGGCGGGCGG 480
ACCACGAGGT CAGGAGATCA AGACCATCCT AGCTAACATG GTGAAACCCC ATATTTATCT 540
ACTAAAAATA CAAAAAAGTT AGCTGGGCGT GGTGGCACAC GCCTGTAGTC CCAGCTACTC 600
AGGAGGCTGA GGCAGGAGAA TGGCGTGAAC CCAGGAGACG GAGCTTGCAG TGAGCCGAGA 660
TCGCGCCACT GCATCCCAGC CTCGGCGACA GAGCGAGACT CCATCTCAAA GTAAACAAAC 720
AAACAAAAAA GACTAAGTGA AGAGGCTTTG GAGATAAAAA CTCCTAGATT TCAATCCCAT 780
CCTGACCTTT CACTAGCTAT ATCACCATGG GCACATTATT CAGCCTTTCT CTGTTTCTCA 840
TTTGTAAAAT GGGGCTAATA CTACCAACAT CATGGGGTTG TAAGGATTAA ATGAGAATTA 900
AACAAGACCA CCAAGCAGCA GGTCTGGCAC CAGGCAGTAT TAATTCCCAC TCCCTCACAA 960
CTTATTGTTA GGAAATGCTG CCTGTCAACT GTGCCAGGCG GCCAGCTAGG TCTAGAACCA 1020
GAGGACTCTG AAAGAGCTGA TCCTGGACGG AAGCAAAGGA TGTGGCTCCA AACAAGCTCC 1080
AAACCAATCT AGACAAGAGT CCTCAAACAT AAGCATACAT AGGGGGAATG TACAATCTCT 1140
CATAGGGAAA TTGCTTCATG AAGGAAACTG TCATCTTTAC ATAAATATTT ACATAACAAC 1200
TGAATGCTCC TCAATCCACT GAAAAACTCC ATCTGACCCC CCTTTGTCCA GAGGCAGGGC 1260
CGTCAAGTGA GAAGACTCAA GAATAATAAG CCCATTCACT GTGCCAAATG GTGGGAGGCA 1320
CCCAGAGTGG CAGAAGACTT CAGGAAATTA AGCCACTCAG CCGGCTGGGA GGCTCTATCA 1380
GCACGCGGCA GGCTGCAGAG CCCAGCACTC ACACCCTGCC CCCTAGGTCG CTGGCTTGGC 1440
TTTGCTGACC CAGTCCGTCC CCTAAAGGGA CTCCTCCCGA ACCTGCTGAA CCTCCACACA 1500
CACCTGCATT CCAGCATTCC TAGATCTCCA CTCCTCTCAC TCTTCAACCA GACTTTCCCC 1560
CCAGCTTCCG TTTCTATCAG TGACTTCAGC TCCTGGCCCT GACTTCCAGG TCAGCTCAGA 1620
CATGTGGGTC CCCCCCACCC CTGATGTCCA ATCACCAAGT TTTAGCTAGT CAGTGTTCCA 1680
AAGGCTCTCA CACACACCCA TCCCTGCCCT ATGCAGGCTG CAAACTAGTC TTCCCATCTC 1740
CAGGGTCTCT TTCTCACAAC CATCCCACCA GGCTCCCCGG ATGAATGTGT CCTATCATGC 1800
TGCTTCCCTA AGGCTGGCTG TCTTGCCCCC CTCCTCCCCT CACCGCCCCC ACCTGTCAAT 1860
GGGTGGCGGC GGGAGGGGTC AAGTAGCCTA ACCAGTCTGG 1900
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