| Tag | Content |
|---|
EnhancerAtlas ID | HS150-01749 | Organism | Homo sapiens | Tissue/cell | NT2-D1 | Coordinate | chr10:48318030-48319260 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr10:48318434-48318455 | CTCAGCACCAGGCACAGTGCT | + | 6.3 |
| | | 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 |
| GH10I047420 | chr10 | 48317360 | 48318926 |
| Enhancer Sequence | GGGACAGGAG CCCTCATGCT TGCCCTCCAC TGGGACACTA GGGTGAGGTG GGCCTCTGGT 60
TGCCCCTGGC ATCAAGTGAC CAAAGGCCGA CACCCATAGA GCCTGCCTTC CTCCAGGGCC 120
CAGGCCTCTG TGGCAGGATC CGGCTGCCCC CTCCTCCCAC AGTCCCAGCC TGGGGGTCAC 180
AGCCCCTCTC CACTGTGCTT CTCACCTCTA TCCCTCTTAT CCTGCACACT CCTTGGCACC 240
CACAGCAATA AACAATCACA GTGGGGCAGG TGTTCACAGG AGGCGGGGGC AGTGGTGATG 300
GAGGAGGAGG TGGTTTCTCC TATTCTGGCT CCTAAAAAAT GAAAAACAGA ACTGTCTGCT 360
TCCTTTCCGG GCAGATCCTG GGTGCAAGGC CATGGTGTCG TTGCCTCAGC ACCAGGCACA 420
GTGCTGACCA CTCCCAGATG TGTATCTGGG GAATGAAAGG ACTAGTGAGG AGCCCACACC 480
ACAGGGGAGA ATCTTTTGTG TGAGAAACAT GCAAACTCCT CCTGGTTTGC AGACATGGTT 540
TTTCCCCTAA ATGCCAACGA CTTCGTCTCT GTCCCTTTGT TTCTTCCGCG GCCAGCCCTG 600
TTGAAAGAGG CCTGCTCTGG GGGCTGTGCA ACAGTCCCAG CATTTGCAGA TGACTGTCTG 660
CATCCACCTG GTTGCAGATG CAGCCTCCCT GAGCCCACTC TGGAGCACCG CAGAGGCCAG 720
CCTTGGCCAG GGAGGCCTGT TCCCACCCCA TCCCAGGCCC AGGGCCTCCT GCGTCAGCTA 780
CTGCCCTCAC CACAGCCTAT GGCCCCTGGG GTGGGTCCCT GGCCCAGAAG CCTGCTTCCA 840
GACTCCTGGC CCCTGTGTTC ACTGGGCTGG GTGTCTCTCC CAGTTCGGTG CCTGCCAGGA 900
CTCCCGCATC CCTAGAAGCT AACCCCAGCC AGCCCCTCGT CCCTGCCAGG AGACAGGGAT 960
CCAGAGAGGC CAAATGGAGC CACATCTGCA TCCGGAGCCT GGGGACGGGG CCAGGTCCCT 1020
AAAACACGGG GCTCCTTTTC CAGAGCGCCT CCGTCCTTAG CATCTTATAC ATGCTCTGTG 1080
GAATATTGAG AGGCGAGCCC CATTTATTCA GGAGAGATCA TCACAGTTGC TGAAACTGGC 1140
CACCCCAGGC TGTGAATTGG TGAGAAGCCT CATTTTGAGG GGTGCAGGGA GTGGGAAGGG 1200
CGTGCTGGGG ACATCACTGT GAGTCCCCAC 1230
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