| Tag | Content |
|---|
EnhancerAtlas ID | HS089-10355 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr5:131634700-131636530 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr5:131635295-131635307 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr5:131635299-131635311 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr5:131635303-131635315 | GTTTGTTTGTTT | + | 6.32 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_09625 | chr5:131628280-131635377 | CD14 | | SE_09625 | chr5:131635907-131639044 | CD14 | | SE_27887 | chr5:131633694-131634935 | Fetal_Intestine | | SE_27887 | chr5:131635955-131638557 | Fetal_Intestine | | SE_28847 | chr5:131633778-131634951 | Fetal_Intestine_Large | | SE_28847 | chr5:131635772-131638825 | Fetal_Intestine_Large | | SE_40097 | chr5:131633497-131635303 | K562 | | SE_40097 | chr5:131636302-131638098 | K562 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I132300 | chr5 | 131636223 | 131638572 |
|
Enhancer Sequence | CCAGGGCCCC TGAGAAGGTT CTCTGCATCC CAGTTGGCAC AACACAGGTA GTGGGACTGT 60
CCTCAGATTG TGTCTTTGCC TTATACTGCC GTGCCAGGAT CTCCCAATGG GCATATCTTT 120
GGGGACAGAC AAGTCTGCCT GAACTGCCCC CCAACACCTC TTCACAGGAG GACAGGGTTA 180
GCCAGGAACC AAGGATGGCA TGCTGTGCTG TAGAAATGCC TTTCATAGTA TGCCAGGAGG 240
TAGCAATAAG GTGTCTGAGT TGGGGTTTGC GTGAGTGCAT TCGTCTGTGT GTGTACATGT 300
GTATAAGGTA GTTTCCTTCT TCAGGGGTTG ATTGTGAGGT CCAAGTTTTT CAACCTGTGC 360
AGTTACTAAG AGTCAAATTA TTTTTCGTTT TATTTTATTT TATTTTATTT TATTTTATTT 420
TATTTTTTTG AGATGGAGTT TCTTTCTTCG TTCTTGTTGC CCAGGGTGGA GGAGTGCAAT 480
GGTGCCATCT CGGCTCACTG CAACCTCTGC CTCCTTGGTT CAAGCGATTC TCCTGCCTCA 540
GCCTCCCGAG TAGCTGGGAT TACAGGGGCC TGCTACCATG CCCGGCTAGT TTTTTGTTTG 600
TTTGTTTGTT TGTTTTTTGT ATTTTTAGTA GAGACAGGGT TTCACCATGT TGGCCAGGCT 660
GGTCTCGAAC TCCTGACCTA AGGTGATCCA CCTGCCTCGG CCTCCCAAAG TGTTGGGATT 720
ACAGGCGTGA GCCACCGCGC CTGGCGATTA TTTTTTAACT TTATTTTGAA ATAACTTTTG 780
ATTTAGAGAG AAGTTTGAAA ATAGTACAGA GATTTCACAT ATACCCTTCA TCTAGCTTTC 840
TCTGATGTTA ACAATTTAAA TACGCGTTAT GCATTTATCC AAACCAGGAA ATTAACATTG 900
GTTACAATAG TAATAACTGA ACTACAGACT TTGTTTGGAT TTCACCAGTT TTTCTACTAC 960
TGCCCTTTTT CTATCGTAGG ATCCCATCCA AAATCCCATG TTGTATTTAG TTGTCATGTC 1020
TCAGTCTCCA ATCTGTGATT GTTCCTTAGT CTTTCCTTAT CTTTCATGAT CTTGACATTT 1080
TTATGAGTAT TTTGATGAAT GCTCCTCAGT TTGGGTTGGC ATGATTTTTC TCACAATTAG 1140
ATTGCGTTAT GCACTTTTTG GTAATGATAC CTTAGAAGTG ATGCATTCTC TGGGCATCAT 1200
ACCAGTGGGT ACATGATGCT GATGTGTCTT ATTACTGGTG ATGTTAACCT TGATCATTTG 1260
TCAAGTTGGT GTCTGTGGAA TTTCTCTGCT GTAAAGGTAC TATTTTTTCC TCTGTCACTA 1320
ATAAATATCT TAAGGGAGGT TCTTCGAGAT TATACAAAAT CCTGTGTCTC CTCAAATTTT 1380
TATTCACTGA TTTTAGCATT CATCACTAGG TCTTGACTGA AACAATTATT ACTGCAGTTT 1440
GCCTAGTGAT GATTTTGCAT TTTCTGATTC CTTCAACATT TATTAATTGG AATTCTTCTG 1500
AGAAGAAGAG CTTCCCCTCC ACATCTATTT ATTAATGTAT GCAATTGTTA ACTTATATCA 1560
GTACAGGTTC ATACATACTT ATTTTATTTC ATCAGTTATA AACTAATGCT ATCCATCTTT 1620
ATTTTGTTGC TCCAGTTATT CTAGCTCAAA CCAAGTTATT TTTCACTTTA AGGATAGAGA 1680
ATGTAGATAT CCAGGGTAAG GGCCTTTATC TGTCTCTGCA GTCAGGGCTA GAGGAGTCTG 1740
TGTTTACCCC TGCGGGAGGA GTGCCAGTCA CAGCTCGTTG CTAAGTTTTC CATCAGGCAG 1800
CAGTTGAGCA GGAACGCAAG CAGGGACTGG 1830
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