| Tag | Content |
|---|
EnhancerAtlas ID | HS147-24327 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr2:198532260-198533870 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr2:198532438-198532449 | AGCTGTGATTT | - | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTATGCATCT GGTGTAACAG CCACTTCTTC CAATTTTTTG AACTGCTTTT GTGGAAAAGG 60
TTTTTCCTGA GGATGTATCT ATGGTGTCGG TTGGGTAGGA TGCTTTGGTT TTGATTCTGG 120
GTGCATGGAA TAGTGTAGTC TCTGTATGAC TTATTTGGCT GTAAACAACA TCAGTTGTAG 180
CTGTGATTTC CATAGAGGCT TACAGTATGG TTATTAGTGG ATGCTGTGGT GAGGTTTTCT 240
TGGGAACTGG GATGCCAGGT AGGCCAGTCT TTGGGCCCCA GTGGTGGCAG CAGTGGGTTG 300
AGCATGCCTG TCTTTGGGAC CCAGTGAGGC ACATGTTGGC ACTGGTGTTA GCAGGTCCAG 360
GTGGGCCAAT TCTTGGACTT CTAGGTAACT TAGTTTTGCC AGTAGTGGTA GCAGTGGGCT 420
GGGTGGGTAG GAGGGTCCTT GGCCCCCTGG GGAGCCAGTG TGGCATGGGT GATTTCAGTG 480
ATAGTGATGG GACAACCTTT GGGTTGCAAG CAGTGCACCC TGGTGTTGGC AGTGTCTGTG 540
GTGGGCTGTG TAGGCCAGTC TCTAGGCCTG CAGGTGGGTG CATGCAGATA GGTGCCAGCT 600
ATGGTGGTAG CAGCCAGGTG GGTAGGTCTC TGGAAGGAGT GTTCAGGTAG CAATGGTGGT 660
GAACTTAGCT GAACCATCCC CTGACCTCTG GGCTGTGTGC TCTGGCATGT TGAGGGGAGT 720
GAAGCTAGGC TAGAGGGGCT GTCCTCAGTC CTCTGATAGC ATGAGCAGGC ACCAGTCATG 780
GTAGGCAGGA GTGGGATGTT CCCCAGGCCA GCAGTGGAAT GTTCAGATTG GGGGCAGCAG 840
TGGCCATGCT GCTGTCCTGC CACTGGGGAG GGAGGTGCTG CCTTTAGTGG TAGCAGCCTA 900
GACAGGTGGG GAACATATGT GATGCTTGTG CCTCGGCCTC TGCTGTGATA GCCTATGCCT 960
TGGTAGCACT TCAGCCCTGG GCGTGGTAGC CTGTGGTCAT TGATGCCTCA GCCCAGAGGC 1020
ATGTACCTGC ACCTGGCAGT AGCCTGCACC TGGGTTGTAC CTCAGGCCTG GCTGCAGTAG 1080
CCTGCATGCA GTCGCTTGTG CCTCAGTCAT AGGGCAACAG TCTGCATTTC TCTTGTGGCT 1140
CAGCCCTAGC ATCACTAGAT CTAGGACAGT ACTTGGTCTA TTAGGGATGG GGCTCTAAAA 1200
TGGTGCCTTG CTGTAGCTGC CTAAGTCTCG GGAAGTGTTT GGGACCCAGT ATGCCCTTCC 1260
TCCCTGGGAC AGTCCTGTGG CACAATCTCT TGGCAGCTCC CTCTGTTAGT TTCAGGGCCC 1320
TCAAGGATTG AGGAACTCTC CCATGGTTAG AATTGCAGGG GTCCACAGTG GGAAGGTGAA 1380
GTACTGAGGG TCTCTCACTT AACCTTTCCC CATACTGGGG AGTCTCTCTC AGGCCTCAGC 1440
TGATCCCAAC TGAACAGGCT GCCTCACTTC CTTCTCCTTC CTTGTTTTAG ATATTTCTTG 1500
TCACTTTTCT GTGGAATTCC AGTGTGCTCT CTTGGATGAT CTACTCAATG TGTGATTATC 1560
TACTCACTGT TTTGGTTCTT CCTAACTGCA GTTTTAAAAT ACAATAAAAT 1610
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