| Tag | Content |
|---|
EnhancerAtlas ID | HS098-13023 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:49671620-49675790 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr12:49671810-49671823 | GAACCTTCCAGAA | - | 6.19 | | IRF1 | MA0050.2 | chr12:49672814-49672835 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | | NKX2-5 | MA0063.2 | chr12:49674223-49674233 | ACCACTTGAG | + | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr12:49673038-49673053 | CGAACTCTTGACCTT | - | 6.06 | | Nr5a2 | MA0505.1 | chr12:49673215-49673230 | GCTGGCCTTGAACTC | - | 8.25 | | PHOX2A | MA0713.1 | chr12:49672764-49672775 | TAATCCAATTA | + | 6.02 | | Phox2b | MA0681.1 | chr12:49672764-49672775 | TAATCCAATTA | + | 6.02 | | ZNF263 | MA0528.1 | chr12:49674505-49674526 | TCCTCCTCCTCCTCCTCCTCT | - | 10.23 | | ZNF263 | MA0528.1 | chr12:49674499-49674520 | TCTTCTTCCTCCTCCTCCTCC | - | 10.29 | | ZNF263 | MA0528.1 | chr12:49674514-49674535 | TCCTCCTCCTCTTCCTCCTTC | - | 10.63 | | ZNF263 | MA0528.1 | chr12:49674502-49674523 | TCTTCCTCCTCCTCCTCCTCC | - | 11.36 | | ZNF263 | MA0528.1 | chr12:49674520-49674541 | TCCTCTTCCTCCTTCTCTTCC | - | 6.84 | | ZNF263 | MA0528.1 | chr12:49674529-49674550 | TCCTTCTCTTCCTCCTTCTTC | - | 7.36 | | ZNF263 | MA0528.1 | chr12:49674490-49674511 | CTCCTCCCCTCTTCTTCCTCC | - | 7.3 | | ZNF263 | MA0528.1 | chr12:49674517-49674538 | TCCTCCTCTTCCTCCTTCTCT | - | 7.71 | | ZNF263 | MA0528.1 | chr12:49674479-49674500 | TTTTCTTCTTCCTCCTCCCCT | - | 7 | | ZNF263 | MA0528.1 | chr12:49674523-49674544 | TCTTCCTCCTTCTCTTCCTCC | - | 8.5 | | ZNF263 | MA0528.1 | chr12:49674508-49674529 | TCCTCCTCCTCCTCCTCTTCC | - | 8.67 | | ZNF263 | MA0528.1 | chr12:49674493-49674514 | CTCCCCTCTTCTTCCTCCTCC | - | 9.38 | | ZNF263 | MA0528.1 | chr12:49674511-49674532 | TCCTCCTCCTCCTCTTCCTCC | - | 9.83 | | ZNF263 | MA0528.1 | chr12:49674526-49674547 | TCCTCCTTCTCTTCCTCCTTC | - | 9.83 | | ZNF263 | MA0528.1 | chr12:49674496-49674517 | CCCTCTTCTTCCTCCTCCTCC | - | 9.93 | | Zfx | MA0146.2 | chr12:49672617-49672631 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr12 | 49674076 | 49674219 | | chr12 | 49672726 | 49672844 | | chr12 | 49673393 | 49674139 | | chr12 | 49673229 | 49674063 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I049279 | chr12 | 49673278 | 49674047 |
|
Enhancer Sequence | TGGGCCCTCG CCCCGTGAAA TAGGTCCCCT TTGCTGACAT CTCATTAGCC TGTCACTGCC 60
CCTTTCATGC CAAGAACCTA GTGCCCCTGA ATTTGTCATT GTCAGCCCCA AGCAGGTTTT 120
GGGAAAACAG TTCTTTCCTC CTCTACACTC CCTCCGAGTC TACAGCAGGA GAGCAATAGT 180
CAGAATCAAT GAACCTTCCA GAACTAGAGA CATGTCTGCT TTAGTCATAA TACAAAAAAT 240
GCTTTTAAAC AGTCGTCTCC CTACTGGACT TTTTTTTCTC TCTCTCTCTT ATTTATTTAT 300
TTATTTATTA TTTTTGAGAC AGTCTGTCTC TGTCGCCAGG CTGGAGTGCA GTGGTGTGAT 360
CTCAGCTCAC TGCAACCTCC GCCTCCCGGG TTGAAGTGAT TCTCCTGCCT CAGGCTCCCA 420
AGTAGCTGGG ACTACAGGCA TGTACTACCA CGCCCAGCTA ATTTTTGTAG TTTTGGTAGA 480
GACAGGGTTT CATCATGTTG GCCATCTCCT GACCTTGTGA TCCGCCCGCC TTGGCCTCCC 540
AAAGTGTTGG GATTACAGGC GTGAGCCACC GCGCCTGGCC TTTTTTTTTT TTAATTGGAA 600
CAGACTATAA AGGTTTTACA GAATATAAAG ATTTCCTAAT TACACAAAGA TTTTGTCTAC 660
AGAAATTAGT TTAACTCATG GAAGAGGGTG GGTATAAATT CAACCCCACT CTCTCTCCCT 720
TCACCCTCTC TGCACACTTC TCTATTTTTT TTTTTTTTTT TTTTTTTTTT TTGAGACGGA 780
GTCTCTCTCT GTCGCCCAGG CTGGAGTGCA GTGGCGGGAT CTCGGCTCAC TGCAAGCTCC 840
GCCTCCCAGG TTCACGCCAT TCTCCTGCCT CAGCCTCCCA AGTAGCTGGG ACTACAGGCG 900
CCCGCCACTA CGCCCGGCTA ATTTTTTGTA TTTTTAGTAG AGACGGGGTT TCACCGTTTT 960
AGCCGGGATG GTCTCGATCT CCTGACCTCG TGATCCGCCC GCCTCGGCCT CCTAAAGTGC 1020
TGGGATTACA GGCGTGAGCC ACCGCGCCCG GCCACACTTC TCTATTTTTA TCAAATATCT 1080
CATTTGGCTT CCAAGAGATG TCTAGTCCAA GAGTAAACAA ATACTGAAAT GCCCTTGGCA 1140
AAGGTAATCC AATTATACTA TTCTGGCAAT CATCTCCAGT TTTTTGTTTG TTTTTCTTTC 1200
TTTCTTTTTT TTTTTCCAAT ACAGAGTCTT GCTCTGTCAC CCAGGCTGGA GTGCAGTGGT 1260
GCCATCTCAG CTCACTGCAA GCTCCGCCTC TCGGGTTCAA GCAGTTCTCC TGCCTCAGCC 1320
TCCTGAGTAG CTGGGATTAC AGGTACCCGC CACCACTCCT GGCTAATTTT TGTATTCTTA 1380
GTAGAGCTGA GGGTTCACCA TGTTGGCCAG GCTGGTCTCG AACTCTTGAC CTTGTGATCC 1440
GCCTGCCTTG GCCTCCCAAA GTGCTGGGAT TACAGGCGTG AGCCACCGCA CCTGGCCGTT 1500
CTTCTTTCTT TCTTTCTTTC TTTCTTTTTT TTAAATTAAG CCTGATACTT GCTAAGTTTA 1560
TTTTTTTAGA GACTGAGTCT TACTATGTTG CCCAGGCTGG CCTTGAACTC CTGGGCTCAA 1620
ACACTCCTCC CACTTCAGCC TCCTGTGTAG CTGAGACAAC AGCACACCGC ACTGGGCTTC 1680
ATTTTCAACT TTCAAGTTTT ATTCGTTCAT TATTTTTGCA ACACCTGTTT GGTGCAAGTC 1740
ACTGTGCTGG GTACTATAGG AAATATATTT AGCTTTTTGC TTCTCAGATT GTAGAGACAG 1800
ACCACACATG CATAATCCCA ATTCGAGGCA GCATATGCCA CATGTCACAG AAGAGGCTGT 1860
CACAGGCAGT AGCCACTGTT GCATAGCTAC TTCAAAGCCA TTCCCAGCTT GTTCCACCTG 1920
CCAACACAAC GCAGCTCTGT CCTGGTGTGG GACACCCATG TGCATTGGAG GGGCTGGGCT 1980
TCACTACCAG GGTGAACCTT CCCCTAAGCC AATCAAGGTA ATTCCAGTTG TTTCGCCAGG 2040
GCCTGGTTAA GGAACCAGCA TGTGATGTAA TTATGGAAAT GAGAGGTGAG GTAATGTCTG 2100
CCGGTTGGGG GTTGGAAGGA AGATATTCTT GCAAAAATTT CCTTGCTCTT AAAAAAGAAC 2160
TCAGGGAAAG GATTTTCCTC TTGCAGCCCT GGGCATTACT GCGTGAGCAC ATTGTGCTTG 2220
TGCTTGTGCT TGTGCCTGGT GCTTGAGGTT GCTGCAGCCG TCTTGTGACC AGAATGGGAC 2280
AAACACGAGG ACAAAAGCTA CCGCTCAATA GCAAGGCAAC ACAGAAAGCT GAAAAGAGCA 2340
TGGGCCCCGA TAGAGTGTTG AGCCCCTGAA TTAACCAACC TTGACACCAA ACCTTGCTCT 2400
GCCTCCGAAG TTTTTACAAG ATTTTTAGTC CCCTTATTGT TTAGGACATT TTGATTTGGG 2460
TCTTCTATTT TTTCCTGCCA AAAGCATTCT AACTAACATT AAAGCCTTAT GTAATTGTTA 2520
ATAGATTTTT TTTTCCTTAT TTTCTGCCGG GCGTGGTGGC TCATGTCTGT GATCCCAGCA 2580
CTTTCAGAGG CTGAGATGGG TAGACCACTT GAGGTCAGGA GTTCGAGACC AGCCTGGGCA 2640
GCATAGCAAA ACCCTGTCTC TACAAAAATA AAATAAAATA AAGTAGAAGA AGCTGGGCAT 2700
AGTGGTGTGT GCCTGTGGTC CCAGCTACTC CGGGGGCTGA GGTGAAAGGG TTTGAGCTGA 2760
GCCCAGGAGG CAGTGAGCTG TGACCGCACC ATTGCACTCC AGTCTGGGCG ACAGAGCAAG 2820
ACCCTGTCTC CAAAAAAAAA AAAAGAATTT TTTTCTGTAT TTTCTTCTTC CTCCTCCCCT 2880
CTTCTTCCTC CTCCTCCTCC TCCTCTTCCT CCTTCTCTTC CTCCTTCTTC TTTTGTAATA 2940
GAAACAGGGT TTTGGCAGGG CACGGTGGCT CACGCCTGTA ATCCCAGCAA TTTGGGAGGC 3000
CAAGGTGGGC AGATCACTTG AGGTCAGGAG TTTGAGACCA GCCTGGCCAA TATGGTGAAG 3060
CCCCATCTCT ACCAGGTGTG GTGGCACACG CCTGTAATCC CAGCTACTCA GGTGGCTGAG 3120
GCAGGAGAAT CACTTGAACC CAGGAGGTGG AGGTTGCAAT GAGTGGAGAT TGCACCATTG 3180
CACTCCAGCC TGGGCTACAG AGCAAGACTC TGTCTCAAAA AAAAAAAAAA AAAAAGAAAT 3240
GGGGTTTCAC CGTGTTGCCT AGGCTGGTCT CAAACTCCTG GACTCAAGAA ATTCACATTC 3300
CTCAGACTCC CAAAGCGCTG GGATTACAGG TATGAGCCAC TGTGCTTGGC CAGAAATTTG 3360
TGGTAAAATT ATTAATAATA AAAATATGAA GGCCCTGCTT TCATTCAGGC CAAAAAATAT 3420
TAAGGCCCTT TTGAATTTGC AGAACCCCTT TGCCAGTGCA AACCTTGCCT TGGGCGAGTG 3480
AAGATCCTGT CCCCTCTTTC TTTCCTCATA TGTTGCCTTC TTCCACCTGC AGTTCCTAGT 3540
CCACCAAATG GATCTGCTTT TTCCTTCCAG TCTTCCCAGG TGCCTTGGCC AAACTCAAAC 3600
CATAAATAAA AGGAACACAG ACACCAGGCA TGGTGGCTTC TGCTGTAATA CCAACACTTT 3660
GTGAGGCTGA GGAGGAAGGA TTGCTTAAGG CTAGGAATTC GAGACCAGCC TGGCAACATA 3720
GTGAGACCCT GTCTCTACAC AAAATGTAAA AATTACCCTG GTGCTGTGGC ACGGACCTAT 3780
AGTCCCAGCT ATTCGGGATG ATGAGGTAGG AGGATTGATT GAGCCTGGGA GATCAAGGCT 3840
ACAGTGAGCC GTGTTCATGC CACTGCACTG CAGCCTAGGT GACAGAGCAA GACCCTGTCC 3900
CAAGGGGGAA AAAAAAAGGA TAGAACATCT GCAAGTCCAA ACAGTGTGCC ATATTCTTCC 3960
TTTTTTTTTT TTTTGAGACA GAGTTTCGCT CTTGTTGCCC AGGTTAGAGT GCAGTGGTGC 4020
AATCTCAGCT CACCGCAACC TCTGCCTCCC GGGTTCAAGC GATTCTCCTG CCTCAGCCTC 4080
CCAAGTAGGT GGGATTACAG GCGCCTGCCA CCATGCCCAG CTAATTTTGT ATTTTTTATT 4140
AGAGATGGGG TTTCTCCATG TTGGTGAGGC 4170
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