Tag | Content |
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EnhancerAtlas ID | HS035-03027 |
Organism | Homo sapiens |
Tissue/cell | Endometrial_stromal_cell |
Coordinate | chrX:70350060-70351390 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chrX:70351198-70351213 | TGAACTCCTGACCTC | - | 6.22 | TBX20 | MA0689.1 | chrX:70350624-70350635 | CTTCACACCTT | - | 6.32 | TBX21 | MA0690.1 | chrX:70350625-70350635 | TTCACACCTT | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH0XI071130 | chrX | 70350164 | 70350780 |
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Enhancer Sequence | CCAGGTAGGC CAAGGCCGTG GGGGCTGTGG AGGAAGCAGT GGGCCCAATC TGGGGAGAAA 60 CAATAGGAAC CTTGAGAAAA GGAGAGGGGC AGTTAAGTAG AGAGGAAGAC AAACAAGGAT 120 ATAGGGGAGG GGAGAGGTAG CGAGAGAAAC AGCTCCAGCA TGGGCTGAGG AGTAAGTCCA 180 GTAGGGTCTA GACTCCAGTG TAAGAGTATT AGGTGAGGGC ATAGCTATCT GGAGTGAATC 240 TAGCTTATCA ATGGGAAGCA TAGCATCTGG GAGGCCTAGG TGTGGGCCGT GTATATTTGG 300 CATTTTGGCC ATGGCTCAGG AACTGAATAG TAATAGCTAC TACTTGCTGA GCATGTGCTT 360 TGTGCCAGGT ACTGTGCTAG GCACTCTGCA CACATTTCCT CATTTAATCT TTATGACCCT 420 ATGAAGTAGG TGAGCCTCCC TGTTTGACCG ATGAGGAAAC TGAGGCTTGA AGAGGTTAAG 480 TAACTTGTCT AACGTCACAT AGCCCATAAG TTTAGAGTCA ATATGTGAAC CCAGACATGT 540 CTGTGCACTT TCCTCTTCAC ATTGCTTCAC ACCTTCAGAT GACCAGAGAG TGGAAAAATA 600 AAGCCGTTGA GGAAAAGCTA AAGGAATAAG GTCTCTTCAG CCCAGAAGAG ATAGTGTTGA 660 AGAGAGATTA GCTAACAGTA GCCTTCTGGT CTCTACAGGA CTTTGAGAGA TTGTCTTATA 720 AAGGTTCTGT CAGGGACTTT GAGCAGCTGG TCTAAAACAA GAGAAGCAGG CTTCAACTTT 780 AACATCAAGG GTTTCAAGGT TAAGCATTAA GCAGAACTTC CTGATACGAA GGGATGGGAA 840 AGATGTGAAA TCTTTCCTGA ACTATTTTAA AAATTGGAAA GATTTTCAAC TAGTTTGGAC 900 TATTTAAATG TAGTCTTTTT TTTTTTTTTT TTTTTGAGAC GGAGTCTCGC TCTTGTCGCT 960 CAGGCTGGAG TACAGTGGTG CGATCTCGGC TCACTGCAAC CTCTGCCTCC CAAGTTCAAA 1020 CAATTCTCCT GCCTCAGCCT CCTGAGTAAC TGGGATTACA GGTCGCCCAT CACCACGCCC 1080 AGCTAATTTT TGTATTTTTA GTAGAGATGG GGTTTTGCCA TGTTGGCCAG GCTGGTCTTG 1140 AACTCCTGAC CTCAGGTGAT CCGCCTGTCT CAGCCTCCCT AAATGTAGTC TTTCTTAAAG 1200 ATGGGGACAT AGAGGTCCCT TTCAGACCTC CAGGAGTCTG TGATTCAATG TTGCAGGAGA 1260 TCAGGAATTG GCCTCAGATT GTTGGGTAGC TGGGGGTAAC ACGATGATGA CTAGCCTGGG 1320 TGTGGGGCCT 1330
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