| Tag | Content |
|---|
EnhancerAtlas ID | HS120-00579 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr1:202003510-202004680 |
Target genes | | Number: 15 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB1 | MA0018.3 | chr1:202004082-202004094 | GGTGACGTCAGC | + | 6.14 | | CREB1 | MA0018.3 | chr1:202004082-202004094 | GGTGACGTCAGC | - | 6.14 | | NFAT5 | MA0606.1 | chr1:202004430-202004440 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr1:202004430-202004440 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr1:202004430-202004440 | ATTTTCCATT | + | 6.02 |
|
| | Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
| SE_23058 | chr1:202003070-202004639 | Colon_Crypt_1 | | SE_23723 | chr1:202003133-202004433 | Colon_Crypt_2 | | SE_23723 | chr1:202004446-202004634 | Colon_Crypt_2 | | SE_24689 | chr1:202003019-202005179 | Colon_Crypt_3 | | SE_25977 | chr1:202003098-202005224 | Duodenum_Smooth_Muscle | | SE_26730 | chr1:202003201-202004852 | Esophagus | | SE_27624 | chr1:202002753-202007729 | Fetal_Intestine | | SE_28545 | chr1:202002635-202005490 | Fetal_Intestine_Large | | SE_31432 | chr1:202003030-202004833 | Gastric | | SE_33417 | chr1:202002752-202008344 | H2171 | | SE_33792 | chr1:202002877-202005297 | HCC1954 | | SE_34304 | chr1:202003057-202005125 | HCT-116 | | SE_34741 | chr1:202002989-202005297 | HeLa | | SE_41626 | chr1:202003359-202004353 | LNCaP | | SE_43434 | chr1:202002760-202004009 | MCF-7 | | SE_43434 | chr1:202004034-202004676 | MCF-7 | | SE_50066 | chr1:202002922-202004883 | Sigmoid_Colon | | SE_52354 | chr1:202003018-202004869 | Small_Intestine | | SE_56834 | chr1:202002917-202004651 | VACO_400 | | SE_57376 | chr1:202003233-202004124 | VACO_503 | | SE_57376 | chr1:202004143-202004423 | VACO_503 | | SE_57945 | chr1:202003251-202004112 | VACO_9m | | SE_57945 | chr1:202004146-202004634 | VACO_9m | | SE_65333 | chr1:202002930-202005541 | Pancreatic_islets | | SE_67013 | chr1:202002752-202008344 | H2171 |
|
| | 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 |
| GH01I202033 | chr1 | 202002815 | 202007566 |
|
Enhancer Sequence | TGCCTCAGCT TCCCCACCTC TCACATGTGG TTGATCCTCA CAGCCATCTC TTGGGGTTGT 60
TCTGAAGATG AAATGAGATC ATCTATGTAA GAAGCTGGCA CTTAAAAGCA CAGAGAGGGC 120
ACCAAGGAAC GTATGGTCTG TCCTTATTTG GGGAATGGGG GTGGAAGGCG CCCAGCAGGG 180
CATGGGGCGT GGTATGGCAG AGCCAGGACT AAGGGTCTGT AGCCTCCTAA ATCAGGGCTT 240
TCTCCGCAGG ATTTCCCATG TTCTCACCAT CTACAGAGTC ACTCCCCTCC ACCCTGCTGC 300
CCCGTTCCAC CAAGTGGCCC TCACACTAGG TGGAGGAGCC CTCACAGATC TCTTTCCTTC 360
AGCCTGCCGT TCTTTCTGCA GCACCAGGGC CCTGGGACCA GCTGGTGGTT TCCACCAGAG 420
CAGCCTCGGG GTGAATTTAG TCAGGAATGT GCCCTCAGCT CAAGAGAACC CTCCCCAACC 480
TTCCACTCCC CATACCCACC CCCGACCGCA GGTTCCCCAC CCACCCGTGG CCTGGCCAGC 540
AGCAACCTCC ACTAGCTCGC TAGCTCAGTG ACGGTGACGT CAGCCCTGCA GTGCAGGCTG 600
GGCTGGTTTA CCCGCAAGTT TCACCTCTCC CTGGGGAGAC TGGATTACCT CACCCTGGGA 660
GCAGAGTGAA TGATTAACCA GCTTCATCCT GGAGGGCCTC AAAGGCCCGT CCTGGGGTGT 720
AGGCCTACAG GGCAAGGGGC TGCATGGTCA CATACCCTAG TATGCGGGTT CACATACCCC 780
AGCCGGGGCT GGGGTATGTG ACCGCCCCGT CCTTGGCCAC TGCCCTCTTA TCTGCATCAC 840
TGCTCACAAG TGTCATAAAA ATTTGTCTAC AGCATATATA AATATACATA TGACGTGGAA 900
GGCTTCCGAT GGCAAATAAC ATTTTCCATT TTGCCTAAGC TTGGGTGGCT TTTTATTCAT 960
CTATTGTTGT TTTAAGTACA CATTTCCATC TAAACTTAGA TGTATGTTTA GGCTGGCCGC 1020
GGTGGCTCAT TGCCTGTAAT CCCAGTACCT TTTAGGGGGT TGAGGCGGGT GGATCATTTG 1080
AGGCCAGCAG TTCAAGACCA GCCTGGCCAA CATGATGAAA CCTCGTCTCT ACTAAAAAAT 1140
ACAAAAATTA GCTGGGTGTG GTGGCAGGCG 1170
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