| Tag | Content |
|---|
EnhancerAtlas ID | HS073-05765 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr17:1480420-1481540 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr17:1481439-1481454 | GGGACAGGCTGACCC | - | 6.32 | | SPI1 | MA0080.4 | chr17:1481159-1481173 | AACTTCCGCATTTA | - | 6.42 | | SPIB | MA0081.2 | chr17:1481159-1481171 | AACTTCCGCATT | - | 6.27 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_09501 | chr17:1477198-1482172 | CD14 | | SE_24303 | chr17:1480428-1481001 | Colon_Crypt_2 | | SE_24303 | chr17:1481005-1481629 | Colon_Crypt_2 | | SE_25267 | chr17:1480380-1481766 | Colon_Crypt_3 | | SE_27390 | chr17:1480364-1481857 | Esophagus | | SE_41871 | chr17:1480390-1481757 | LNCaP | | SE_50860 | chr17:1480343-1481848 | Sigmoid_Colon | | SE_53184 | chr17:1480354-1481865 | Small_Intestine | | SE_68949 | chr17:1480336-1481912 | H9 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I001573 | chr17 | 1477152 | 1482396 |
|
Enhancer Sequence | GTTCTGGGAT TACAGGCGTG AGCCACCGCG CCCGGCCCTG CTGGGTGGTT CTGCAAAGTG 60
TTTCTCTTTG GACCAGCTCC AGGCCCCAGA CTCTGGGGAG GGCCCACCCC ACTCAGCTGT 120
GCCCAGGGCC TGTGGGTGTC TGGCTGAGCC GAGTGGAAAG CGTGGTGCCA GCGGGGACCT 180
GCGGTTTGGG AAACAGGCCC AGAGAGGAGT GTGGAGGCTG GGCTTGGCTC TGCAGTGCCC 240
TCGTCCAGAG AAGCATTGAG TAATCGCGGA AACTCAGCAC CACAGATCCC GCCCCCCTCC 300
CTCAGACCCT GCCAGGACAG CCACAGCTTC CTCCAGGCCT GGGGAGGGGC AGGCGGAGGG 360
CAAGCGGAGC TGGGATTACC CCAGGGGCTG TTGCGGGAAT TGGGAGAGAG TTCCGGGCTA 420
AATCTTAGCA CATGTCAGGC TCTGCTGGCC CAGAGGTGGG AAAGGAATCC CAGCAACACA 480
TGAGCTGGTC CCACATCAGA GACTGTGGAT GATGATGTTT GAGTTTCAGT TTTTGGGTCA 540
AGGCCTGAGC CAGAGAAGAA GGAACCACTG TGGTTCCTTT TATGTTTCTG GGGCTTCTTG 600
GAAAAAGATA CAGGTTTCAT TTTAGCCAGG GCTGGAGAAA GCTATGGCCA GAGCTGGGCG 660
CACTGAGGCT CTGGATGGGC CCGTCTGGTG TATTCTGGAC TCAGTCACCC ATGTTGCTGC 720
CCGTGATGAG GGCAACTGGA ACTTCCGCAT TTAGCTTCAG GCAGCCAGAA CCTACCCATC 780
CTTCCCAGTG AGCAGCCAGG GCCAGCCCCA GGACTCGGCT GTAGTGGCCC CTGAGGCCAT 840
AATGAGCTGC ACAGGTGCCT GACCCTGGCT GGGGGAACTG ACTTCGTGTT GAATGCCAAG 900
GCTTGTGAGC ACCCAACTGT CTGCCCACTG ACCTGCTTCC CACGAGGTAT GGCCTTTCCC 960
TGAAACACCC AGCAGAAACC CTGGTACCTG TCCCCTGAAG CAGGAAGATG AGCCCTTCTG 1020
GGACAGGCTG ACCCTGCCTC AGAGTCTCAG TCCCACCAGC AACCTCCCCC CGGCCATTCC 1080
CACACCCTCG CCCACCAGGC CACCTGCGGC TTCCAGGACT 1120
|
