| Tag | Content |
|---|
EnhancerAtlas ID | HS007-08417 | Organism | Homo sapiens | Tissue/cell | BE2C | Coordinate | chr19:48873770-48875200 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr19:48875141-48875153 | GTTTGTTTGTTT | + | 6.32 | | NR2F1 | MA0017.2 | chr19:48874764-48874777 | AAGAGGTCAAGGG | + | 6.14 | | USF1 | MA0093.2 | chr19:48874199-48874210 | GCCACGTGACC | + | 6.62 | | USF2 | MA0526.2 | chr19:48874197-48874213 | CAGCCACGTGACCCCA | - | 6.68 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 48874226 | 48874554 | | chr19 | 48873906 | 48874015 |
| Enhancer Sequence | GTGGAGCCTA TCCAGGAAGA GTTCCAATTC TAACGAAGGG GAGATTTTCT TTTTCTTCTC 60
TTTTGAGACA GGGTCTCACT CTGTTGCCCA GGCTGGAGTG CAGTGGTGCG ATCACAGCTC 120
ACTGCAGTCC AGACCTCGTG GGTTCAAATG ATCCTTCCGC CTTAACCTCC CAAAGCACTG 180
GGATTACAGG CATGAGCCAC CACACCAGAC CAAAGAGAAG ATTTTCAACA GTCTGTTTCC 240
CTTAGCCTAC CCCCGCCATC CCCAACCCCT ATCGCCAACA CTGCCACTTC CAATCAATCA 300
CCAAGTCCTA TTTTACACGC TAAATATTAC TGAATTCCCC AGGGCTCTGG CCTCAGCCTT 360
TCTCACCTGG GCCTCCCCGC CTCCTCTCAG GTATGTTGGC CTCTTGTCTT GCCCACCTCC 420
GATCCATCAG CCACGTGACC CCAGAGGGCT TCTCTAACCC CAAGGCTGAC CCCAGCTGTC 480
CCCTGCACAG AATCCTCCCA TGCATAATAT TGAATGCTTT CCATGGCTCC CCAAGTCCGG 540
CTCCTGGCCC TGGTGTTCCG GGCCTCTTAG AGCCTGGCTC CCACCCACTT TTCCAGCCTC 600
ATCTCACACC AGAACCCTCC AGTGAGTTTC TCTCTTATCT CTGAAACTGC CCGCTCTGCA 660
GCATCTGGCT TTTCCACATG CCATCCACCC TGCCGGGAAT GCCCTTCCTC CTCTTGTCTG 720
TCTGAGAAAC TCCTTGTTCT TTAAGGTCCA GTTCAGAACT CACCTGAAAT CCAGCCCTCA 780
ATCTGGCTTC CACCTTGACT CTCTCCCCCA CCCCAGGCCC CAGCCTCCTC CCCACCACCC 840
CATCTACACA CCAGCTCGTC TTTGTCTGGC ACAGACCTGC CCTGCTGCAT TGTGACCATC 900
TGGGACAAAT CACTGGGGCT TCAAATTTTC ACCGAATTTC GTTGATAGGA GCCCCCGCCC 960
TCAAGGCGCG TGGTCCAGTG TGAGGAAGAA GAGCAAGAGG TCAAGGGCAG ACTCAGAAGC 1020
CAGGCTACTT CTGTTCAAAT CCAGGCTCTG ACACTGACCA GCTGATTTTT TTTTTTTTTT 1080
TTGAGACAGG GCCTCACTGT GTCACCCAGC CTGGAGTGCA GTGGCACAAT CAGGGCTTAC 1140
TGCAGCCTTG ACTTCTGGGT CTCAAGTGAT CCTCCTACCT CAGCCCCCCA AGTACTTGGG 1200
ACTACGGGTG CATGCCACCA CACTGAGCTA ATTTTTTTTT TTTAAGAAGT TTTGGTAGAT 1260
ACTAGGTATC ACTCTGTTGC CCAGGCTGGT CTCCTGAGCT CAAGCGATTC CTCCCACCTT 1320
GGCCTCCCAA GTGTTGGGAT TACAGATGTG AGCCACTGTG CTTGGCCTTT TGTTTGTTTG 1380
TTTTGAGACA GAGTCTTGCT CTCTCGCCTC GGCTGGAGTG CAGTGGCATG 1430
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