| Tag | Content |
|---|
EnhancerAtlas ID | HS141-00145 | Organism | Homo sapiens | Tissue/cell | NB4 | Coordinate | chr1:11443620-11444890 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LHX2 | MA0700.1 | chr1:11443674-11443684 | GTTAATTAGT | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 11443709 | 11444800 | | chr1 | 11443705 | 11444695 |
| Enhancer Sequence | CACTGGTCCG TGATATCAAT AAGACACATT GGCCCATTAT ATCAATGACA TCACGTTAAT 60
TAGTCTGGAT GGGCAAGAAG TGGCAAGTGA TTTGGAAGCC TTGATAGGAC AGACATGCTT 120
CGGAAGGTGG GGACTCCCTA TCAGTGAAAT TTTTAGTACA GTGGTTTGGT TTGGGGCACG 180
CCAGGACATC TCCTCCAAAG GAAACCACAA GTTGTTGCAT CTTGCACCTC CCACACATCA 240
GAAGGAAACA AAACATCTTA TAGGCCTTTT TTGGGTTCTT TAAGCAATAT ATTCCACACT 300
TGACAAATAC TGCTGCAACC CATTTTGCCA AGTGCCAAGG ATGGCTGCCA GCACTGAGAG 360
GGGCCCAAGG CAGGAGAGGG TTCTGCAGCA GCTCCAGGCT GTGGTACAAG CAAGTCCCAC 420
GTCTGGAGTC ATGTGACCCA GCAGACGTTG ATAACAGACA TATCTGTGGT GAGAAAAGAC 480
GCTACGAGTT TATGGCAAGT CCCAATAGGA GAATAACAAC ATAGATCCCT AGAGTTCTGG 540
AACAAGGCCA TGCCATCTGT AGTGGAAAAT CATGCATTAT TCGAAAAATA GCTTTAGTGT 600
GCTTCTGGGT CTTGATAGCG GTGGAGCGTC TGCTCAGCCT GGTACAGACA GCTTCGACAT 660
GACACCCTGT GAGCATGGAG AGTCATCCCC CAGAACACAG AGCACACCCC AAATGAATGA 720
CCATACTATT CTATGGTGTT GTGTCTGCAG TAGGTAAAAC ACGTGGTCTG GAAGCTAAGG 780
GGTGAAAGTA ACAGAGCCAT CACTCACTGT CATCCTCAGT GACTCATTTA GGAAATTCAT 840
TTCCTGTCCC TGAAACTTTA AGCTTTGTGC GTCTGAAGAT CTGCTCTGGT TTCCAGATGG 900
GGAACGCTTC ACCAGGGTAT AGAGTAAGAG CTCCCCCAAA CTTTAACCCA CATCTGCCAC 960
CTGGTCATTT CAGATTCCTT GGACCAAAAG GCCATGGGAC GAGGGAAGGA GTCACTGTAC 1020
TGGCAGGAAT TACTGTCCCT GAGCAACTGG CAGGAGAAGG TAGGATTGCT GTTACACAAT 1080
GAAGGCAGGG AAGATCAGTT TTGGTACCCA CGTGATCTGT TGGGCTGTCT TTTGTTATCC 1140
TCTTGCCCAT TTTTGACAGT AAATGGGTAA GTGTGGCAGC CATGAGCTGG GAAGGGCACA 1200
GTTACCAGGG AGGGGCCAGA CCTGTGAGGG ATGAGGGTCT GGGTCATCCC ACGAGGTGAA 1260
CTCTAGATCA 1270
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