| Tag | Content |
|---|
EnhancerAtlas ID | HS128-01678 |
Organism | Homo sapiens |
Tissue/cell | MCF-7 |
Coordinate | chr1:201153240-201154950 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GLI2 | MA0734.2 | chr1:201153625-201153640 | GGATGTGGGTGGTCC | - | 6.19 | | RELA | MA0107.1 | chr1:201153925-201153935 | GGAAATTCCC | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I201184 | chr1 | 201153928 | 201154528 |
|
Enhancer Sequence | TCTAGGCTGG CCAGGGGGAG TGAGGGTTCC TGGAAATAAG TTATGTCCCC ATCAGCCTCA 60
ATTTTCACCT CAGGTAAATC AGTCCACAGG CATTAAGCTT TCCCTGAGCG TGTGCCCAGG 120
CTTGAGCACA GGGGTTGGGA GTCCCTGTCC CTGCCCCTGG GAGCCCCCAG TCTGATGTAG 180
GAGACATGGC CCCTACACTT GAGAGTCAAG TCCTGGTTTC AGAATTTTTT CTACTCCAAT 240
CTAACCAATG CACACCACCC ACGGGCTCTT TCTAGCATAC AAATATGTTA TCTCTCTGCC 300
TGAGAGCCTC CCATGACTCC TCATCCACTC CAAAATAAGT GCCAAACTCC ATAGCAAAGT 360
ACAAATGACA CTTTACAGCT TGCCTGGATG TGGGTGGTCC TGTTGGTAAT GGGCTCCTTC 420
CTGTCATGTC AAGAAATATG ACCTGCTTGA AGCTTGTTTT TGGGAATCTG CTAAACACAT 480
GTTTAGCCAG GACTGTCTTT TACTTAAAGG GAACTCTTCC TTGCAGGGTG GGGATGGGAA 540
AGGGCCTATA TAGCTTCTGA GCATCTCCCG ACTCCGGGCT CAAAAGAAAC TGCCTTGTCA 600
TAAAGCTTCT GTGATCAGAG CCGTGTCCTT GGGTGTGGTG GGCTGTGGAA AGGTGAAATA 660
GAAGGAGAGG CAATTCTGGC TCTTGGGAAA TTCCCAGGAC TCAGAAGGAG ACAGAGTGTC 720
TGCAAGACAG ACTGAGACCT AAAAACTGAG GTGAATTAAT GCAGTCACAT AGAAATGCCA 780
CTTAATATGG TGACCACAGG AGGGCAGGGA GGTCAGCATT CCAGGCAGGA GGGAGAACGC 840
AGTGGGGACG AGAGGCCAGC CTGCCTGAGT TGGAGGGAAC ACGCTGGGAG GTCAGCGGTG 900
AGAGTGTTGG TTGGTGTAAT GCTCTGGATG CCGGGAAGAG TTCAGATTTG TCATAAGCCA 960
GGCTCTATGC ATGGGCAGGA GAGTGCCCTC TTCAGCATGG AAGAGCAACT CCACTCCAAA 1020
TCCAGCCTGA CAGAGTCTGT TTCTAATAGA AGAGTCTGAG TCAGGTTGTC CGGCTTGGGG 1080
CTTCCAGGAG ACAGTTCCAG GACTCGGGTC TCCTGGCTCC CCTGCCCCAG TCTGCCTCAG 1140
GGTCTCCCAA CTCAAGGTGG CTGGCTCCTC CAAATTGCCT CACTGCTACT TACCCAGCAT 1200
TCTAGCTCCT TTTGGACTCT GTTTCTGCAC CTGAGAAAAT GGCTTTCAGC CCTGGGTTCT 1260
AAGAGTTGCT CAGGGCAGTG ACTTAGCTGA GAGCTGGGTG AGGATTCCAG GGGACCGCAA 1320
GGTGGGTTCT GCAGTCCCAC CCCTCCCCAT CTCCTGCCAG CATAAAGCCT CTTGCTGCGA 1380
GGCCCAGGGC CACTAGGAGA AGTAGCAGTG GTGGTTGTCA GAGGCACGTG GCATGGCTGC 1440
TCTGAGCTGT GGGGGCAACA GCCCCAGCCT CCTCACCGCT CTTGGGAGAG ATGGGTAGAA 1500
GGGCACCTTT TTCCCAGCGA CTTGCTACCT CCTTCCTCTC TGCCAGCCTC TAGGCCAGTC 1560
TTCCAAGGCC ATTGTGAGCT GGAGCCACTG TGCGGAGAGA GCCAGGGCCT GGAAGGGGTG 1620
AGGCAGAGCC TCCTCTAACC TCCTGCAGAC CTGCCTCCCT TGCTGGGCTC CTGCCCTAGA 1680
CAGAGCCTGT CATGGCAATG GGGATGGGGT 1710
|
