Tag | Content |
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EnhancerAtlas ID | HS095-25487 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr6:8084580-8086050 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ALX3 | MA0634.1 | chr6:8084762-8084772 | TTTAATTAGA | - | 6.02 | LMX1B | MA0703.2 | chr6:8084708-8084719 | AATTTAATTAA | + | 6.32 | Nr5a2 | MA0505.1 | chr6:8085455-8085470 | TGTGGCCTTGACCTC | - | 6.09 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_38648 | chr6:8079665-8087031 | HUVEC |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr6 | 8084831 | 8084926 | chr6 | 8084979 | 8085194 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I008079 | chr6 | 8080034 | 8087367 |
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Enhancer Sequence | TGAATATTTT GCACTATAGG ATTATGACCT TATTCATTCT GCTGGCAAAG GAATTCCAAA 60 CAAGTTCCCT CCTTTTCCGA GTATTTCTTT TCCCTACTGC AAAACCTGCA TAAGCTAGAG 120 GAAAAGAAAA TTTAATTAAA CACTTGGTTT ATGAGTTACA CTTCAGTATC ATCTTTTTTA 180 TTTTTAATTA GATGTAGAAA TACTCTCCTT CTTAATGACA GCCCGATGCT ACAGCAAGCA 240 AGATCTTGTG GGTCTGAACA GACGTTCACT AGCCTGCTGG CTGTCATCAC AAAGGACGAC 300 TGATGATATT TTTCCTAATA TAAAGCTTAA AAAGTTAAAT GTCAAACCAT ATGTCACATT 360 TAAATATATA TTTCGTAAAA AGCCAACAAG TTTGTTATTG TGGTTTTCAG ATAGAAATTG 420 TTCTTGGAGC CCTGTTGGGT AGCCATGCTC ACAGCAGCAC AGTCTCACTA AAATGAAGTA 480 CAGACTCCCT CAAGTTCAAA GACTGTGTTT AGGCTGCCAC CAGGAGAGAG ATGCTTAGAT 540 ACCTTAGCAG CAAATCCTCT TTACCTTGCA GGCTTTTTTT GTTTTGAAAT GAGGTAAGTT 600 GTGCCTCATG ATCATTTTAA ATTCGAAAAG CTACTAAAAC ATATTGAACC TAGCATGGAA 660 TAAAAGAAGG TGGTAATCAA TGTACTTCAG CTCCAATAAA CTTTCTCCAC ATTTAAATAA 720 CATTACTTAT ATTACACTTT CACTACAGAG ATAAAAAATC TGAAATAGGA ACTATAAATA 780 GGTACCAGTT GTTAAATATT GCTTTTATTT ATTTTTTTAA GACAGGTCTC ACTCTGTTGC 840 CCAGGCTGGA ATGCAGTGGT GCAATCATGA CTCACTGTGG CCTTGACCTC CCTGGGCTCA 900 GAAGATCCTC CTACCTCATT CCCCCAAGTA GCTGGGACTA CAGTCACAGA GCTACCACGC 960 CTGGTTAATG GTTTTTTTTT TTTTTAAATA GAGACGGGTT TTGCCCTGTT GCCTAGGCTG 1020 GTCTTGAACT CCTGGGCTCA AGCTATCTAC CTGCCTCAGC TTCCCAAAGT GCTGGGATTA 1080 CAGGCATGAG CCATCATGCC CAGCCTTAAT ATTGCTAATC TCAATAAGCA TTTAGCTGCA 1140 CAAGGCACTG TTTTAAAAGC CAAGAGGGGA TGAACAGAAA TAAGACAAAT CCTCTTTGGT 1200 CTCTTATTTT GTGTAAATTG AATCATATTC TTTGTAAGTA TGGGGAATAT TCATTCTACT 1260 TCACTCCTGT TGTCCCAATG TAATTATTAA TAGGCCTCCT TTCACAGCCA AGTGTTTTGG 1320 ATGAGAAATC ATGTGGTCGC CCTATTTACA AAGAATATTT GTAATCAAAC TTATCATAAG 1380 CTTTCCAAAA CAATGAAAAT TCCCTTAGAC AGCCAAGGCC ATCCAAATCT TCAGATATTT 1440 TTCTGACAAT TTTCTGATTC TGTATTCTAC 1470
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