| Tag | Content |
|---|
EnhancerAtlas ID | HS118-05014 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr12:122487520-122491510 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr12:122489999-122490014 | TGAACTCTTGACCTC | - | 7.64 | | RARA(var.2) | MA0730.1 | chr12:122489285-122489302 | TGACCTTGCTTTGAACT | - | 6.02 | | RARA | MA0729.1 | chr12:122489996-122490014 | TCTTGAACTCTTGACCTC | - | 6.45 | | ZIC1 | MA0696.1 | chr12:122488314-122488328 | CACCCCCTGCTGAG | + | 6.29 | | ZIC3 | MA0697.1 | chr12:122488314-122488329 | CACCCCCTGCTGAGA | + | 6.36 | | ZIC4 | MA0751.1 | chr12:122488314-122488329 | CACCCCCTGCTGAGA | + | 6.04 | | ZNF143 | MA0088.2 | chr12:122488219-122488235 | CTGTGCATTGTGGGAC | - | 6.65 | | ZNF263 | MA0528.1 | chr12:122490398-122490419 | TTCTCCACTTCTCCCTTCCCC | - | 6.07 | | ZNF740 | MA0753.2 | chr12:122490774-122490787 | GGGGGGGGGGGGG | - | 6.03 | | ZNF740 | MA0753.2 | chr12:122490775-122490788 | GGGGGGGGGGGGG | - | 6.03 | | ZNF740 | MA0753.2 | chr12:122490776-122490789 | GGGGGGGGGGGGG | - | 6.03 | | ZNF740 | MA0753.2 | chr12:122488202-122488215 | GTGGGGGGGGGGC | - | 6.29 |
|
| | Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
| SE_01319 | chr12:122488563-122489854 | Adrenal_Gland | | SE_43043 | chr12:122488483-122489946 | Lung | | SE_46444 | chr12:122488765-122489931 | Osteoblasts | | SE_46977 | chr12:122488674-122489387 | Ovary | | SE_47525 | chr12:122488639-122489739 | Pancreas | | SE_48380 | chr12:122488161-122490709 | Psoas_Muscle | | SE_51670 | chr12:122487832-122491016 | Skeletal_Muscle | | SE_52996 | chr12:122488686-122489721 | Small_Intestine | | SE_53888 | chr12:122488668-122489877 | Spleen | | SE_54716 | chr12:122488205-122490012 | Stomach_Smooth_Muscle | | SE_65468 | chr12:122488044-122490116 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr12 | 122488969 | 122489119 | | chr12 | 122490073 | 122490175 | | chr12 | 122490667 | 122490766 | | chr12 | 122490816 | 122490894 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH12I122050 | chr12 | 122488535 | 122490046 | | GH12I122052 | chr12 | 122490281 | 122490430 |
|
Enhancer Sequence | GAGATTGCAG GTTCATGCCA TTCTCCATAT CAACTATAAT ACTTCCCGTT CAAGTCTGTG 60
ACTGTGCCAT AATTTATGTG AACAGTCCCT TAGTGATGGT CACTTAGGTG TTCCCGTCTT 120
TTGTTTTGCA CATGCAGTCC TGCGGGGGGT CTGGTACCCT CATCTCTCTT CACTTTTGCC 180
CAGGTGCAGG TGGCTCTGCA GGCTGCGTCC CTGGAAGTGG AACCGTTTAG TCAGAGGCTG 240
CATATGCACT CAGAATGTCA CAGGTTCTGC CTGGCTTTTC CCCCCGAGAA GTCATGGGTA 300
GGATGACACC ACTAGCACAG GGGTTCTCAG CCTCAGCACC CCTGGCATTT GGAGACGGAT 360
CATTCTTTTT GTTTTTCTGA GACGGAGTCT CGCTGTGTCA CCCAGGGCGG AGTGCAGTGA 420
TGCAATCTGG GCTCATTGCA ACCTCTCTGC CTCCCGGGTT CAACTGATTC TTCTGCCTCA 480
GCCTCACGAG TAGCTGGGAC TACAGGCGTG CATTTGCCAT CACACCTGGT TCATTTTTGT 540
ATTTTTAGCA GAGACAGGGT TTCACCATGT TGGCCAGGCT GGTCTCAAAC TCCTGACCTC 600
AGGTGATCCA CCCGCCTCAG CCTCCAAAGT GTTGGGATTA CAGGCGTGAG CCACCACAAC 660
CAGTCTTGGA TCCTTCTTTA TTGTGGGGGG GGGGCCATCC TGTGCATTGT GGGACATTGA 720
GCAGCATCTC TGGCCTCCAC CAAAATGTTT CCAGTTGTTA ACCAATGTCC CCAGGATAGG 780
GGCAGGGGTA AAATCACCCC CTGCTGAGAG CCAGTGCCCT AGCGGCTTTG CCATAGCCTT 840
CGCTGCGTAC AGTATGTGTC GTCCCCTCTC ATCTCCCCTC ATGGCCCCCG TGATCCCAGC 900
ATGCCCACCA GGCTTCCCTG GAAGGTGGTT CTGCAGGTAG AAGGCAGAGG GGGTGAGACG 960
GGGGCTGTGG TCACATACAG GGGGACACTC ACCAGCTGTG TGGGCCTGGG CAGGAACATC 1020
ACCTCCACAC ACCCTCCTAC TTCCTTGTTT GTAAAATGGG ATGACCAGCT ACTCGGGAGG 1080
CTAAGGTGGG AGGATCACTT GAGCCTGGGA GGTGGAGGCT GCAGTGAGCC ATGATCGTGC 1140
CACTGCACTC CAGCTTGGGC GACAGAGCGA GACCCTGTCT CAGCAGAAAA TAAAATGGGA 1200
TAAACAGAAG CTGCCTCCCT CGCCGGGAGC GAAGGGGGCG AGAACGCCAG CAAAGTGCTC 1260
GGCCTGGAGC TGGGGCTTAG GAGGAGGGTC TGGGAGCTGC AGGGTTGCCT TGTCCACCCT 1320
TCTGTCGGGG GAGCGATTGC GGGGTTCCCA AGGACGGACA TGGGCTTCGT GTGCAGCCGC 1380
GTTCCTGCTT CTTTCCCATC CTGGTTTCTT TCTGGCCGTG GCCTTGTTTC TCCCACGTTG 1440
GGGGTGTGTG TCTCCTTTGC TCTAGAAGCC CGATTTGAGC TCCGCAGCAG GAATTATGTT 1500
TTGAGTTAGT GTGTCCAGTT GGTTGCTACT TTCTCGCCAC TACCACCAGA TGCTAAATTG 1560
GTGGGACGCA GGTGGGACCT CCACCAGGGT CCTCTCTGGC CACCCCAGGC CCCTGGGCCT 1620
GCACGGCTGC CCTGCACTGC TCAGCCAGGA TCCACCTGCC TGCTGCCCGA GCTGCCCGTG 1680
GGAAGGGCAC AAGGACAGAC CCGTGTGGCC TTCCCAGGTG GGTGCGTGCT GTCTGCCGGG 1740
ATGGGGCAGG TCGGCCACCA GCTGTTGACC TTGCTTTGAA CTTGTTTACT GCTGTGTGAG 1800
TTCAGGGAAT GACATAATTC CTGTCCAAGC TCCCTGGACT AAATTTAGGT CCCAGGAAAA 1860
TAATTTTCCC TGGGTGAGTT CCAGCACCGC AGCGCCCAGA GAATCGGCTG CTGCCCTGAG 1920
CTCCTGAATG CTCTGTGGGT TCCAAGGCCA GTTCCCACCA AGCTCTAGGG CCTGGCTCTC 1980
AGGAGAGGCC TCTGCCGGGC ACCTCTCTGC CCAGCACGGG TCAGCGTGAG TCTCTGGGTG 2040
ACTGGCCACC TTCATGATTT CTAAGCCTAC ATCTGGGGCA CCCACCTCCC CCACCACTCT 2100
GCAGAGCCTG CTGTGCCCGG CAGAAAAGGA GCTGTGGTCA GATCCAAAGC CACAGATGGG 2160
CAACTTTTCT AGTAAAAACT TTAAATATTT ATGTTAAAGC AAACATTTAT TATGAAATAG 2220
AGTATAACAA TAACATGATT TCTCTCTCTC TCTTTTTTTT TTTTTTTTTT TTTTTTTGAG 2280
ACAAAGTCTC ACTCTGTCAC CCAGGCTGGA GTGCAGTGGT GCGATTTTCC GCTCACTGCA 2340
ACCTCCGCCT CCTGGGGTCA AGCGATTCTC CTGCCTCAGC CACCCGAGTA GCTGAGATTA 2400
CAGGCACCTG CCATCACACC CAGCTACTTT TTATATTTTT AGTAGAGACG GGGTTTCACC 2460
ATGTTGGCCA GGCTGGTCTT GAACTCTTGA CCTCAAGTGA TCTGCCTGCC TTGGTCTCCC 2520
AAAATGCTGG GATTACAGGT GTGAGCCACC ACGCCTGGCC TGGCCTGGCC CCTCTCTTTT 2580
AAAAAAAAAA AATAAATAAA CTAGAGATGA GATTTCACTA TATTTCCCAG GCTGTTCACA 2640
AACTCCTGAG CTCAAGCTAT CTTCCCACCT TGGCCTTCCA AAGTGTTGGG AGTACAGGTG 2700
TGAGCAACTA CACCTGGGTG ATTTTTCTTT TTATTGAGAT GAAATTCACA TAAAATTAAC 2760
CAGGTTAAGT GAATAATTCA CTGACAGTAC ACTCACAAGG TTGTGCAACC ACCACTTCTA 2820
TCTGGTTCCA AAACATTTTA ATCACCCCAG AAAGAAACCT TGCACCCAGC CGCAATCATT 2880
CTCCACTTCT CCCTTCCCCA GCAACACTGG GTCCCTGCCC AGGGCAACCA CGAAACTTTC 2940
TGTCTCCATG GGTTTGCCTA TTCTGGACTT TTCATATAAA TGGAATCATA TACTCTGTGG 3000
CCTTTTGTGT CTGACTTCTC ACTCAGCATA ATGTTTTCTT TCTTTTTGTT TTTTTATTGT 3060
TTTGTTTTTT GTTTTGTTTT GTTTTGGAGA CAGAGTCTCA CTCTGTCACC CAGGCTGGAG 3120
TGCAGTGGCA TGATCTTGTC TCACTGGAAC CTCCGCCTCC TGGGTTTATG GGATTCTCCT 3180
GCCTCAGCCT CCCAAGTAGC TGGGATTACA GGCGCGCGAC ACCACGCCTG GCTTACTTTT 3240
GTATTTTTTT AGTCGGGGGG GGGGGGGGGT TTGCCATGTT GGCCAGGCTG GTCTCAAACT 3300
CCTGACCTCA GCCGATCCAC CCACCTTAGC CTCCCAAAGT GCTGGGATTA CAGGCGTGAG 3360
CCACCGTGCC TAGCCTGTTT TTGTTGTTGT TGTCGTTTTT TGAGACAGTC TTACTCTGTC 3420
GCCCAGGCTG GAGTGCCGTG GCATGATCTC GGCTCCCAAT CCAGGAGGTG GTCCTGGGTT 3480
CAAACGATTC TCCTGCCTCA GCCTCCGAGT AACTGGGATT ACAGGCGTGC ACCACCATGC 3540
CTGGCTAATT TTTGTATTTT TAGTAGAGAC GGGGTTTCAC CATGTTGGCC AGGCTGGTCT 3600
TGAACTCCTG ACTTCAAGTG ATCCGCCTGC CTTGGCCTCC CAAAGTGGTG GGATTATAGG 3660
CGTGAGCCGC CGCGCCCGGC CAGGGCTCCT AGTCTGAGAA GTAAGTGTCA ACCCTGCTCA 3720
GACTCCCTGG GAAGGAGGGT CTTGCTGTCC CGTTCCCCCG CCCTCTGTGT CCCGGCCTGT 3780
CCCAGGCCCT GCACTGTCTC CTTCTTCTTC CCATCTTGCC TGCTTGCTTT TAAACTTAAG 3840
CATGGGTTAT TTTCCCCTTT GTTATTACTC TGCCTCAGAA ACCCCAGCAG GGAAGTCTTG 3900
GTCGCACAGG CATTCTCTAG GATTCGTTTC GTGTGTGCTT TTTAACATCA GGGTACCATG 3960
GTGTCCGGGC CTCGGGTAGG ATTTTTGCTG 3990
|
