| Tag | Content |
|---|
EnhancerAtlas ID | HS095-09281 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr14:74513130-74514630 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-5 | MA0063.2 | chr14:74514232-74514242 | CTCAAGTGGT | - | 6.02 | | SOX10 | MA0442.2 | chr14:74513444-74513455 | TTCTTTGTTTT | - | 6.62 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGCGGCATGA GCTTGGCTCA CTGCAACCTC TGCCTCCCGA GTTCAGGCGA TTCTCATGTC 60
TCAGCCTCCT GAGTAGCTGG GATTACAGGC ACCCACCACC ACACCTGGCT AATTGTTGTA 120
TTTTTAGTAG AGACAGGGTT TCGCCATGTT GGCCGGGCTG ATCTCGAACT CCTGACCTCA 180
AGTTATCCAC CCACCTCAAC CTTCCAAAGT GCTGGGATTA TAGGCATGAG CCACCGTGCC 240
CAGCCTGCAC TTGACTTTGG TTCTCAACAT GTATACTAAC TAACCGTAGG AAGATTTCTT 300
ACCTTTTTGT TTGATTCTTT GTTTTTGAGA CAGGGTCTGG CTCTGTCACC CAGGCTGGAG 360
TACATTGGCA TCATCATGGT TCACTGCATC CTCCACTGCC TGGGCTCAAG TGATCCTCTC 420
ACGTCAGCCT CCAGAGTAGC TGGGACTACA GGCATGTGCC ACCACGCCCA GCTAATTTTT 480
GTATTTTTTG TAGAGACTGG GTTTTGCCCG GGCTGGTCTC GAACTCCGGG GCTCAAGCAA 540
TCCACCCGCC TCGGGCTTCC CAAGTGTTGG GATTACAGAT GTGAGTCACT GTACCAAGCC 600
ACATTTCTTA ACTTTCTTGA AGTTAAATTT CTTCAACTAA AAGTAGGGCT AATTTACTTC 660
TTCCAGTAAT CTGAGTTTAT AAAAATAAAT AAATAGTAAA ACCATGGCTA ATAGTAGCAA 720
TCTTGCAGGG TTGTCATGAG GTATATTAGT GGAAGTACAT CTAACTCTCA GGTCTTAATG 780
GTTTATTTCT TGTTCATCGA ACAATCCTGT ATGGGTCTGG CAGCTCTCCT CCAGGGATGA 840
TTCAGGAACC TGGCTGCTTC CTTCTTGCAC CTCTGCCGTG TTGGAGTTTT TCACGTCTAG 900
TCATGTGGAC AGGAAAGAGC ATGGGAGACT CATACCTGCT CTTAACTGCC TTGCACTAGA 960
AGTAACCCGT CCTTTTTCAC TTTATTTATT TATTTATTTA TTTATTTATT TATTTATTTT 1020
TGAGACAGGG TCTCGCTCTG TCACCCAGGC TGGAGTGCAG TGGTACAATC ATGGCTCACT 1080
GCTGTAGCCT TGACTTCTTG GGCTCAAGTG GTTCTCCTTC CTCAGCTTCC TGAGTAGCTG 1140
CGACAGACTA CAGGTGCAAA CCACCACGTC TGGCTAATTT TTTAGATTTT CTGTAGAGAT 1200
TGGGTCTCAC TATGTTGCCT AGGCTGGTCC CAAATTCCTA GGCTCAAGTG ATCCTCCCGT 1260
CTCAGCCTCT CAAAGTGCTG GGATTATAGA TGTGAGCCAC TGCATTCAGC CATTTTCACT 1320
TTTTTATTGG GTGAAAACTT AATTACAAGA TTCCCACATA ACTACTGAGT ACCCACCATA 1380
AGCTAAATAG GTGGTAGTCA CTATTGATAA TATTGGGGGT GCAGGTGGTG AAGCAATCAT 1440
TTTTCTATTT TGGCGATATC TAAAAGTTAG ACCTGTGTTT TGAGATCTTA TATCTATTTC 1500
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