| Tag | Content |
|---|
EnhancerAtlas ID | HS129-03518 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:223575250-223577150 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr1:223577097-223577108 | AGGCCATAAAA | + | 6.02 | | MIXL1 | MA0662.1 | chr1:223575976-223575986 | TCTAATTAAC | + | 6.02 | | NFAT5 | MA0606.1 | chr1:223576637-223576647 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr1:223576637-223576647 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr1:223576637-223576647 | AATGGAAAAT | - | 6.02 | | Stat6 | MA0520.1 | chr1:223576374-223576389 | CTTTTCCTCAGAAAT | + | 7.27 |
|
| | 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 |
| GH01I223402 | chr1 | 223575388 | 223576530 |
|
Enhancer Sequence | CTGAAAAGGC ATGCAGTAAA GACAGTTATT TGTTTAATGC CCCTCCCCCC TTTTTTTCTC 60
AGATAATTTC ATGGAATTGA TGTTCTGTGA AACATTTTTG GAAACAGCAC TCTGTAGTTC 120
CTATATGATT GTGAACTTCT TTGGCCTTCC CTCCCTGTGT TGATAGGAAG TGTTTATAAT 180
TCCATCAGCA CTATGTCTTG ACTGTTCCAC CACAGCCAGG CCATCTGATA TAGTTTGGCT 240
GTGTCCTCAC CCAAATCTCA TCTTGAGCTG TAGCTCCCGT AATTCCCAGG TGTTGTAGGA 300
GAGGCCTTGG GAGATAATTG AATCATGGGG GTGGGGTTTC CCCCATACTA TTCTCATAGT 360
AGTGAATAAG TCTAAAGAGA TCTGACTGTT TTATAAGGGG AAACCCCTTT CACTTGATCT 420
CATTCTCTCT TGTCTTTCAC CTTCCACCAT GATTGTAAGG CCTCCCCAGC CACATGGAAT 480
GAGTCCATTA AACCTCTTTC TCTGTATAAA TTACCCACTC TTGGGTAAGT GTTTATCAGC 540
AACGTGAAAA CAGACTAATA CATCATCTAA GAGCTCATTA GAATCTATTT GGTCTGCTTC 600
TTTTTTTGGT CAGTCCTATC CAGTCTTATG AAATAAAATT CTATTGGAAT CCTTCTCTTC 660
CCCTCTATTT CTCCTCTGTC TCTTTTGGAG GAGGTATGTG ATGTCATTCT GTCTACCCAC 720
ATTGTGTCTA ATTAACCTAA CCAGGCCCTG AGTCAATGAC TAAGCATGAC TCAGTAATAT 780
GACATTTTAA AAATAAGGAG CCAAAAGTTA AATAGAAATT AACCCATCAT ATCTCAGAGT 840
CTTCATTGAA ATCTCTAAAT GCTTTCTTTA AAAAGCCCCT AGTGTCACGT TTGTATTAGA 900
GAGAGAGAAA TAGAATAAGC CCCATTGGGA GATTTATATC TTATTAGTAA TTCTAAAACA 960
TTAAAGGTAA CCTGACAAAG GATTTTGTGC AGAGGTCAGT TTGAGGTCCA CTTTCTTGGC 1020
TCTTATCATG GAAACCACGC CCTCTTCCCC ATTCCATTTT CTTCCCCTGC CCCAGATCCC 1080
TTCTGCCTGG TATGCCCAAA GAGGCCTACT GTAGGACCCT TACTCTTTTC CTCAGAAATG 1140
TTCAGGGACA GCCCCCTTGC TCAAAATGGA AGGGCTCACA TATCTTGCCT CAATTTCCAA 1200
CCTTATTCTC TTCTCCTTGC CCAAGTTAAT CCTCTGTTCC GGCCAAATGC CATGTGCAAC 1260
CCAAATATTC AAGAGTAATG CTTAAGACAT TTCAGACAGA CTTTGTTATG AATCCTAGCT 1320
CTTCCTCTTA GTACAGTTGT GTGAGACTGG AGAAGTTACC TTTTTGAGCC TGTTTTCTTG 1380
TTTGTAAAAT GGAAAATAAT TCGTACTTCA AAGGCACGTT GCAAAGGATG ATAAAAACTA 1440
ATCCATGTAA GGTGTTTGGC ACAGTGCCCA GAACCTGATA CATACCCTAT AGTTAAGTAC 1500
TGCAGGGTTT TTTGGTTAAT AACACTGATC TTGCACCTTT CTCAGTTCCA TTATCCCTAC 1560
TTTGGTGTCT TTTCCCCAGC TGCCCCCTTC TACCATATCC ATGCCTGGGT TTTCTGAGCT 1620
TAGTTCACAT TCTGCCTCTT CCCTGGCTGC CCCATCTTGA CATCACTCTT CACTGACAAA 1680
CTGCATGGCT CATGGAGTAC TTAGTAGTTA CTGCTTGTAT GGCATACCTA TTTTGCAATC 1740
CACATCTTGG CTTCCTAACT AGCCTACATG CTACTTGAAG CCAGGATCAT CGTCTTAGAC 1800
TTCTTTATAC AGTACTTAAC ATGGTGGTCA ATACATAGTC AAAATAAAGG CCATAAAACA 1860
GGATGTTTTG ACTTCACCTC CATATCCCAT GCATTTTTTC 1900
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