| Tag | Content |
|---|
EnhancerAtlas ID | HS128-19634 |
Organism | Homo sapiens |
Tissue/cell | MCF-7 |
Coordinate | chr6:123118300-123119970 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arid5a | MA0602.1 | chr6:123118461-123118475 | TTAATATTGATAAA | + | 6.16 | | POU2F2 | MA0507.1 | chr6:123118424-123118437 | TTCATTTGCATGT | + | 6.92 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_29458 | chr6:123118332-123121457 | Fetal_Intestine_Large |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I122797 | chr6 | 123118484 | 123121777 |
|
Enhancer Sequence | ACTTCATGAG AAGTTGTATC AATAGTGAGT TTTCAGAATA AAATTATCCA GTTTGTGGAT 60
GATTAATTTA TGTTTTCCTT CATAATCTTC TTCAATTTCT CTTTTCTTTT GAGTAATGTT 120
CTGGTTCATT TGCATGTCCA TGACAAGGTT AGCAAGTAAG GTTAATATTG ATAAATATTT 180
ACTTTTTCCA GAATTCTTAT TAGACCTACA AGGATGTGCA TACCCTGATG TAAGCTAGAC 240
TGTAAATAAA AACAAAAACT TACAAATTGC CATAAGAAGC AAAGAGGAAG GAGGTCCATG 300
TTCAAGTCAT AGTTTATCTA ATTAAGACAT GATTCAAGGC AGAAACCATG TTCAGAGCAT 360
TTAATGCCTG AGATACCCCC GGCTCAACAG GTTTTTATTT GAGAACCAAC CTGTGCATAA 420
CAGCAAGATG GCCGTCCGGT TTACAGCATC CTATTGTAGT AGTGTAAAAT CTTAGATTTG 480
TACCCAGAGA TTTTTGTTTA AGTCCAGGGC TGGGCAATTG TCTCCTGTGG TACAAATTCA 540
GCCTGTTGCT TGTTTTTGTA AATAAAGTTT TATTGGAACA CAGCTATGTT TCCATTCATT 600
CTACATTGCT TTTGATTGTT TCATGTTTCA GAATAGAGCA GTTGAAATGG ATAGAAAAAG 660
TTTGCTGACC CCTGGTCTAG ACCTACCCTT CATTTTGTAG GTGAGAAAAT GAAGGCTCAG 720
AAATGTGAAT TACTTGTCCA AGTGCTCCAC ATCCCTTGGG AGCAGAGCCC ATACGCTAGA 780
TCTTTTTACC TCAGATCTGT GTTCGCTTAA ACCAACATCC TTTTGCACAT CCCTTGCCTT 840
GCCTGATTAA CATACTCAAT ATTTCCCAAA CATATCTACT TTCACGCCTC TCTGTGTCCA 900
CATTTTTCTC TTTGCTTAGA ATATCTTCCA TCTCATGTCA AATGAATGCT GAACGGGGGT 960
TTTGATTATT TTTAGTTAAT CGAACCTGAA TACAGTAATT TTGATGAGTT GTATTCTAGA 1020
ATAAGCTTAA GTTTCCAGTG ACTTCTTGTC CCTGGCCTAC TATCTTGAGA TGAGTAATAT 1080
GTGAGTCCTT TTGAGTCAGC CTGTCAACGA GCATTTGTTC CTGTTGATAT GTTAGACCAC 1140
ACAGTGAAGA GGCTTGGGAA CAAATGAGCT CCAGCAGCCC AAGGTCACAC ACATTGTGTT 1200
TATATGCCTT AGGTGGCAGG AAGACTGGAA TATTGGAAAA CACAGGTGTT CATAGTCACT 1260
AGAATGTAAA TCTTTAACCA GCCCTGCTTT CCACTCCCTC CCTCTCCGCC ACCACACCTC 1320
CCTCCCAGCC CTGCTTTTAA TAGCTTGGCC AACTCGGGTG ATTCACTTAA CCTCGCTGAT 1380
GCAGAGATCA CTCATTTGTA CATAGAAGCT AGAAATACCT ACCTTGCAAA GCTTTTGTGA 1440
GCATTGGTGA TATGAAAAAG GCATAGCTTA CTATCTGGCA CAGCATCAGC CCTCAGTAAG 1500
TGGGCTGGTG GTGATTGTCA CATTAAGTGG TGACAGGGGA TACATGTTTG TAACTCCTTT 1560
GAGGATTTGT TTGATTTTAT TTTTATCTCT GTCCTCTTTT TGTCAAGTCA GATCTTACAA 1620
TTCAAAGACA GAAATGCTAC CTAACTTCTA TAACATATCC TATTATATTA 1670
|
