| Tag | Content |
|---|
EnhancerAtlas ID | HS092-15789 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr14:50479240-50480720 |
Target genes | | Number: 21 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Six3 | MA0631.1 | chr14:50480050-50480067 | GCAAGGGTATCACCTTT | + | 6.17 | | USF2 | MA0526.2 | chr14:50479324-50479340 | GTGGGTCACGTGGGCC | + | 6.41 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_28581 | chr14:50479707-50481032 | Fetal_Intestine_Large | | SE_33820 | chr14:50479139-50481593 | HCC1954 | | SE_34553 | chr14:50478882-50481541 | HCT-116 | | SE_35844 | chr14:50478776-50481591 | HMEC | | SE_43464 | chr14:50479094-50481383 | MCF-7 | | SE_47176 | chr14:50479005-50480290 | Panc1 | | SE_57680 | chr14:50479160-50480398 | VACO_503 | | SE_57680 | chr14:50480440-50481370 | VACO_503 | | SE_64483 | chr14:50479218-50481263 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I050012 | chr14 | 50479052 | 50481628 |
|
Enhancer Sequence | GGATTACAGG CATGAGCCAC TGTACTCAGC TAAGGCTGGT TTTAAAATCC TCTCATTTCT 60
CCTAGAAGAT GGTGAGGATG TGATGTGGGT CACGTGGGCC AGGCTCGGGG GGTCATGGGC 120
AGCACACTGT CCTTGGAAAC AGCAGCAGTG GTGCCTCCTG TTTGTTCCTG TCACCTCTTG 180
CTTCCTAGCT GAGCCTCTGC CTCAGTGTCC CCTCTCCAAG ATGAGGCAAC TGCATGTGTG 240
TCCTGCAGCT CCCTCCCTCC CTTGCACTCC TAGCTGCTAG AAGCAGTCAT ATCTGTGAAT 300
CACATAGAGC TCCCTGACAT CTGGTCTTAC ATCAAATCTT TCTTGGCAAT ATAAGAGTGA 360
AACATCCAGT TTTTCAAACT GGCTGTTTTG TTTTGAATTC ATCTTCAGAT GAGCTTTTCT 420
CAGGAGAAAT GAGGAGTGGG GGACAGAGAG CAGAATAAAA TGCCCACAGG AGAGTAAAAC 480
AAGATGCCAA AAGACCAGGA GGAAGACCAC AGATTTCCAG AGCCTGATCC TCTGCCACCA 540
GACCCTGAGG GCAGCTCTTT GATTTCTGGT CACTCGTGTC CTCCATTCCA TGCCTTCGGC 600
AGCCACCACC ACAACCCCGG GGTCGGGCAC CTCCACAGTG TACAGCAAGT TTACTACCTA 660
GCAAAGTATG GCCCAGATCA ACGGGGGCTT CAAAACCATC CACACTTACG TTTCATTCAT 720
TCATTTGCTA ATTTATTCAT TCTATATTCA TTCAACACTC ATTGAGCACC AGTAGGTGTC 780
ATCTAGAAGT CTTGTCTCCA TTTGCTATCA GCAAGGGTAT CACCTTTTCT ATACAATGAG 840
TCTCATTTCC CAAGAGTGGT TTTGGATTTG AAAGCAGATG TTACTCAGAA CCTTTTCTGA 900
GGGCAGTGTC TCAGCTCCCC AGGGAGGCCT CCAGTTCTCC AAAGGAGCCT TATACATCTT 960
TGGCCCAGGT TAGCATCCAT CTCCCTGCAC ATCCTCACAG ATATTAAAAA GGATCAAAGC 1020
ATCTTTGGAC AGTCCCGGGT TGTCTCCAAG GAAATCGGAG GCACCTGGAT GTAACTAACA 1080
AAGACTCTTT GTGTCAGTGG GGCTGAGTCA CCTGACAGGT CTGAAATGTA ACTTCCTCCT 1140
CTGGGGCCAG GAGAATGGAA TCCGAAAGGC TAGAAGGATA GATCAAAATG AAGATAAAAT 1200
TTTAAAGGAA TGAAAGTAGA GTTTTGTACT TAGTGATTAA AAGAAGAAAA GAAATGACGA 1260
AGGAAAAAGG AATCCCATTT GACGGTGTTG TATGTGAAAC TGACTTAGAG ATTTTGGTTG 1320
ACTGCAAACT CAAGGTGGAC TAAGGCCTGA TGTGGCAGCT GGAAACCTGA ATGGACTTTG 1380
ATTGTGTCAC AGAGTCAGGA GTGTCTAGTG AGGAGACAGT AGCCCCCTGG GTTTGTCACA 1440
GGTCAGGCCA TTTGTAAAAT ATTAGGCTTA GTTGTGGGTC 1480
|
