| Tag | Content |
|---|
EnhancerAtlas ID | HS098-14746 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:121399340-121401040 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr12:121400894-121400905 | GGTGACTCATG | + | 6.62 | | JUND | MA0491.1 | chr12:121400894-121400905 | GGTGACTCATG | + | 6.02 | | KLF13 | MA0657.1 | chr12:121399603-121399621 | AGGAAGGGGGCGTGGTCT | - | 6.34 | | KLF14 | MA0740.1 | chr12:121399606-121399620 | AAGGGGGCGTGGTC | - | 7.64 | | KLF16 | MA0741.1 | chr12:121399608-121399619 | GGGGGCGTGGT | - | 6.14 | | Klf12 | MA0742.1 | chr12:121399605-121399620 | GAAGGGGGCGTGGTC | - | 6.08 | | NR2C2 | MA0504.1 | chr12:121399970-121399985 | AAGGGGCAGAGGGCA | + | 6.11 | | NR2C2 | MA0504.1 | chr12:121399989-121400004 | TGGGGGCAGAGGGCA | + | 6.14 | | SP1 | MA0079.4 | chr12:121399607-121399622 | AGGGGGCGTGGTCTC | - | 6.7 | | SP3 | MA0746.2 | chr12:121399607-121399620 | AGGGGGCGTGGTC | - | 6.29 | | SP4 | MA0685.1 | chr12:121399605-121399622 | GAAGGGGGCGTGGTCTC | - | 7.09 | | SP8 | MA0747.1 | chr12:121399607-121399619 | AGGGGGCGTGGT | - | 6.52 | | YY1 | MA0095.2 | chr12:121400341-121400353 | GCAGCCATCTTG | - | 6.74 | | Zfx | MA0146.2 | chr12:121400926-121400940 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_23495 | chr12:121399446-121401714 | Colon_Crypt_1 | | SE_24673 | chr12:121399766-121400584 | Colon_Crypt_2 | | SE_27808 | chr12:121395970-121401773 | Fetal_Intestine | | SE_28751 | chr12:121395949-121401811 | Fetal_Intestine_Large | | SE_32255 | chr12:121399704-121400633 | Gastric | | SE_53251 | chr12:121398282-121401007 | Small_Intestine |
|
| | 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 |
| GH12I120958 | chr12 | 121396119 | 121401634 |
|
Enhancer Sequence | ACTACTCGGG AGGCTGAGGC AGGAGAATAG CTTGAACCTG GGAGGTGGAC GTTGCAGTGA 60
GCTGAGATCA CGCCACTGCA CTCCAGCCAG GGCGACAGAG CGAGACTCCG TCTCAAAAAA 120
ATAAAAGTAA AAAAATTTTT AAAAAGTCCT AGAGTACACA GTTCCTGAGT CTGCTGACTG 180
TCTAAAGATG TTCTTCTCTG ATTTCTGCTG ACTGCAGAGA AGAACAGGGG ACTTTGGTCT 240
CGTTCGTTGA CTCCTCAGCA GGGAGGAAGG GGGCGTGGTC TCTGGTTCTC CAAGGCATTG 300
GCTGGAACAA CAGGAGTTTC CATGCCAGGC TGTAGCTGGT TTTCTCTCAA CATATTTAAA 360
ATTAAACGTG TTTCAAACCA TAAAGTTCAA TTTCCTTCTG AAAACATTCT CCTCTATCTT 420
CTGAATAGGA AACTGATATT CCTGTGAGTT ACAGCACTTT GATTTAATGT TATGAATCCT 480
GATCTTATTA TGCTAAGAGG ACACTGCTCC CTCCCTGCTC AGAGTCATAT GACAAAGACT 540
TCGCATGTCA GTACCCGCAG TGAAGGGGGC CAGGCCCAAC TGGCTCCTGT ACATGCGTGC 600
GTGCGTGTGT GTGTGTGTCC CTGGCTACAG AAGGGGCAGA GGGCAATCTT GGGGGCAGAG 660
GGCAATCTTG TTTGACCGGG CCACATTTAT TAAGTACTTA GGACTGTGTC TAGCACATAA 720
TAAGTGCTCA ATAAACGGAG ATGCCATGAT CATTTGTAGC TAGTTACATA CCCAATATCC 780
ATTCTTCCTA TTTTTTTCCT TAATAACAGA TTCAGATCGT GCTGCCTGGA ATGAAGACAT 840
TTCCCAGTCT CTCTTGCATT TTGGTGTGGC CCCGTGACTA CACTATGTTC CATGGACTGT 900
AGTAGGTAAA AGTGTATGAG GCTTCCAGGA GCCTCAGCCT TGAGGTTCAC TGCTTTTGTC 960
CTCTATTCTA CCTGGTATTT GGATATAATG GCTAGAGTCC AGCAGCCATC TTGGACCATG 1020
AGGTAACCCT GAGTACAGAA GCCACCCACT GAAGATGGTA GGGCAGGAAG GTCAAAGCTC 1080
TGGTGACACT GTGGAGCCCC CACACTAGTC CTGGACTGCC AGCTTCTGGA AAGAATCAAC 1140
TCCTACATGT TTATGACATT TCACTTTGCA GTGGCATCCT TGATAATGTC AGGAGTTTCC 1200
TGGTCCTGGA AGTGATCAAA CAGGCTTTTT AGAGATGATG AGACATGAAA TCACTCGCTG 1260
ATTCATTCTT CATATGTTTA ATGAACACTC ACTGCTAGGT GCTAGGGCTT GTTCTAGTTA 1320
TGAACAAAAC AGAGACTTTA TGAAGCTTAC AGCCTGGAAG AGGAGATGCA TACACCCTCA 1380
CAAATGTGAA AAAGCACCCT GAAAGAGCAA ATACAGTGCA GGGATGGAGA GTCACAGAAA 1440
AGAATCTGTT CAGATGTATC ACGAAGGGCT CTGTGCAGAG GTGACGTTTA AGCTGAGAAG 1500
TAGGATGTCT TAGTCTGTTC CTGCTGCTAT AAAAAAATAC CATAGGCCAG GCATGGTGAC 1560
TCATGCTTGT AATCCCAACA CTTTGGGAGG CCGAGGCGGG AGGATTGCTT GAGGCCAGGA 1620
GTTCGAGACC AGCCTGGCCA ACATGGTGAA ACCTCGTCTC TACTAAAAAT ACAAAAATTA 1680
GATGGGTATG GTGGCGGGTG 1700
|
