| Tag | Content |
|---|
EnhancerAtlas ID | HS197-06556 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr14:55573440-55576410 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr14:55575108-55575119 | GATGAGTCACC | - | 6.32 | | IRF1 | MA0050.2 | chr14:55576267-55576288 | GTCCAGTTTCAATTTCTTTAT | + | 6.01 | | JUND | MA0491.1 | chr14:55575108-55575119 | GATGAGTCACC | - | 6.62 | | ZNF263 | MA0528.1 | chr14:55575036-55575057 | GGAGGAGGGCGAGGGGAGAGG | + | 7.74 |
|
| | Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
| SE_00244 | chr14:55563236-55576350 | Adipose_Nuclei | | SE_00820 | chr14:55574748-55575102 | Adipose_Tissue | | SE_02600 | chr14:55573844-55576160 | Astrocytes | | SE_09388 | chr14:55568067-55576360 | CD14 | | SE_23110 | chr14:55574129-55575416 | Colon_Crypt_1 | | SE_23790 | chr14:55574594-55575269 | Colon_Crypt_2 | | SE_24786 | chr14:55574109-55575428 | Colon_Crypt_3 | | SE_26013 | chr14:55573672-55575878 | Duodenum_Smooth_Muscle | | SE_26711 | chr14:55573567-55575917 | Esophagus | | SE_27630 | chr14:55573899-55576071 | Fetal_Intestine | | SE_28543 | chr14:55573873-55576230 | Fetal_Intestine_Large | | SE_31668 | chr14:55574018-55575868 | Gastric | | SE_33558 | chr14:55573897-55579764 | H2171 | | SE_34039 | chr14:55574107-55575498 | HCC1954 | | SE_34802 | chr14:55573592-55576155 | HeLa | | SE_36310 | chr14:55573891-55575863 | HMEC | | SE_37768 | chr14:55573433-55575974 | HSMMtube | | SE_41170 | chr14:55573962-55575665 | Left_Ventricle | | SE_42472 | chr14:55573658-55575611 | Lung | | SE_44570 | chr14:55573874-55576148 | NHDF-Ad | | SE_45117 | chr14:55573558-55575933 | NHLF | | SE_46036 | chr14:55573692-55576091 | Osteoblasts | | SE_46880 | chr14:55574151-55574573 | Ovary | | SE_46880 | chr14:55574627-55575401 | Ovary | | SE_49010 | chr14:55574074-55575920 | Right_Atrium | | SE_50181 | chr14:55574075-55575919 | Sigmoid_Colon | | SE_52430 | chr14:55573656-55575984 | Small_Intestine | | SE_56717 | chr14:55573869-55576081 | u87 | | SE_57551 | chr14:55574279-55575356 | VACO_503 | | SE_64542 | chr14:55574036-55575714 | NHEK | | SE_66903 | chr14:55573897-55579764 | H2171 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr14 | 55574264 | 55575347 | | chr14 | 55574465 | 55575376 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I055097 | chr14 | 55563775 | 55576469 |
|
Enhancer Sequence | GCTGAGCTTG ATAAAAGATT GCAATGGTTA TGCCTGTATT ATTTCAAATT TTGGTGTTCA 60
TCAAAATGGT AATTTTTCTC ATAGATTGAC TTTATGAGAA GTGAATGCTA AATGAATTTT 120
AACTTAAATG TAGATTCATA AATTATTTCT TTTGTGTTTT TATCTTTTAT TGTTTTTTGA 180
GACAGAGTCT CACTCTGTTG CCCAGGCTGG AGTACAGTGG CTTGATCTCG GCTCACTACA 240
ACCTCCACCT CCTGGTTCAA GTGATTGTCC TGTCTCACCC TCCCCAGTAA CTGGGATTAC 300
AGGCGCCCAC CACCACACCC AGGTAATTCT TGTGTTTTTG TAGAGGTGGG GTCTCGCCAT 360
GTTGTCCAGG CCGGTCTGGA ACTCCTGGCC TCAAGCGATC TGCCCGCCTC AGCCTCCCAA 420
AGTGCTGGGG TTACAGGCGT GAGCCACTGC GCCCGGCCTC CTTGGTATTT TTATGTCTAT 480
TTTTTTAGAT GGAGTCTCGC TCTGTCCCCC AGGCTGGAGT GCAGTGGCGC GATCAGCTCA 540
CTGCAACCTC CACCTCGCGG GTTCAAGCAA TTCTCCTGCC TCAGCCTCCT GAGTAGCTGG 600
GATTACAGAC GTCCATCAAC ACGCCCAGCT AATTTTTGTA TTTTTAGTAG AGATAGGGTT 660
TCACCATGTT GGCCAGGCTG GTCTTGAACT GCCTACCTCA GGTGATCCAC CCACCTTGGC 720
CTCCCAAAGT GCTGGGATTA CAGGCGTAAG CCACCTGCGC CTGGCCGGTA TTTTTAAATT 780
AGAGTTCTTC TAAGATTTAT CTGAAAAAGT TACACTACTA AAAAATTTGC AACCCACACC 840
CAAGGACATA ATTTGTCTGG GCATAGAGAC TTGATGGCAC TTCAAGTAGC TGGATGAGCT 900
TCTCTTAACA TGCGATTTCT CTCAGGTTTA CATTCTTCTT GACTGCCCTT GTTCCTTTCC 960
TATTCTATTT GAAGCAAAAT GGTTAACGTT CTTCCACTTT CACCAGGACA GCCCTATTTG 1020
CCCCTTCCTT GTCCTTGTTA GCCTGGTTTT ATAAAGCCTC TTTTGCAGGG GTCGGAACAG 1080
TTAATAGCAT TGGGGATTGT CGCTTGTTCC CTGTAGATGA AAAGTATTTT TCTATTGTTT 1140
AAAAAAAAAT CGAGGTCATT CTCCAAAGTA ATTTCCTGAA ATAAAGCGTG GGAGGAAGTC 1200
ATGGGCATGA GGATGAGTCA TCAGGCAGCA GCACGAGGCT GCAGGCGTGA GCTGGGGAGC 1260
CCTGGCTCAG TCCTCCGCAG GCTTGGATCC CTGAGCGGAG CAGGCCACTG GGGCCTTCTG 1320
CCGTGAGAAG AGACCTACTG AGAGGCGGGG AGTGGGGGTG GGAGTGGTTG CTTCTGACCT 1380
GTAGGACAGT GGTCAGCGTG GGCGGGTGGA GGCACAGGAG AAGGCCGACA GGCCCTGGGT 1440
CCTAGGGCCA CTCAGCTGCT GGAAAATGAA GTTCAGAGTT GTTTGGACTG TCTGAAGTAG 1500
GATAGAACCA GCCTTAGCCC TAGTTAGGTA ACACATGGCA GAGGCACCTG AGCAAAGACG 1560
TGAGCTGGAC CATGGGCTTC CTGGCAGGAC TTCCACGGAG GAGGGCGAGG GGAGAGGAGC 1620
AAGGGAGCAG AAGGCAGCTT GCCGTCCACG AAGCCTCCTG AGGCCCCAGA TGAGTCACCA 1680
GACAACAGCC TGTCTACTTA AAGCAACTGC TGGGCAACTG CTGAGTAGAA CAGTCCCTAA 1740
CCACATGAAC ACTGGGGAGG AGGTTCTGAA AGACGCTGCT GGGTGCAAGG TCCCTAACTA 1800
GGGTAATCCA ATTTCACTCC AGGCTAACAT GAGAAATTAT GACTCCAGCA GCCAATCCTG 1860
TGGGCCGTGA GAGAGTGGGA GAGGGATTTT CCAGATATAA GTCCCACTAG AGCTTCTTTT 1920
TTTTTTTTTT TTTTGATACG GAGTCTCACT CTGTTATCCA CGCTGGAGTG CAGTGGCACC 1980
ATCTCGGCTC ACTGCAAGCT CCGCCTCCCG GGTTCAAGCG ATTCTGTTGC CCCAGCCTCC 2040
TGAGCAGATG GGACTACAGA TGTGCACCAC CATGCCCAGC TAATTTTTGT ATTTTTAGTA 2100
GAGACAGGGT TTCACTATGT CGGCCAGGCT GGTCTCGAAC TCCTGACCTC ATGATTCTCC 2160
TGCCTTGGCC TCCTAAAGTG TTGGGATCAC TGGCATAAGC CACAGCTTCC GGCTGAGTCC 2220
CACTAGAGCT TCTAAGAAGA AATTAGGGAA GCAGGATTAT GAGAGGCCTG GTCCCACTCA 2280
CAGTGTGCGA CATCACTGAT GACTATGCTT GGTTACCTGC CTTGTTATTT GCTACCTTTG 2340
TTATTGTCTA TTTCTTGGTA ATTAGTAGTA CACTATAGTG ATTAGGAGTG ATCAAGAAGA 2400
TGCCTGGCTT CATATTCCAA CTTTGTCGTT TACTAACTGT GAACTTGGCC GAGTTTTTTT 2460
TTTTTTGCTT GTTTGTTTTG TTTTGAGACA GGATCTCTCT CTGTCACCCA GGCTGGAGTG 2520
CAGTGGCGTG ATCTCAGCTC ACTGCAACCT CCACCTCCTG GAATCAAGGG ATCCTCCCAC 2580
CTTAGCCTCC CAAGTAGCTG AGATACACGT GTGCACCATC ACACCTGGCT AATTTTTGTA 2640
TTTTTTGTAG AGATGGTGTT TCACCATGTT GCCCAGGCTG GTCTTGAAGC CCTGGGCTCA 2700
AGCCATCACC CACCTTGGCC TCCCAAAGTG CTGGGATTAC AGGCATGAGC CACCTCCTGA 2760
CCTCAGGTGA TCCACCTGCC TCAGCCTCCC AAAGTGTTGG GATTACAGGC ATGAGCCACT 2820
GTGGCCAGTC CAGTTTCAAT TTCTTTATTT GTAAATTTGT AATAATGACA GGACTAGCTC 2880
TTAGCCAGAA GCAGCAGCTC TTGCCTGTAA TCCCAGCACT TTGGGAAGTT GAGGTGGATG 2940
GATCACTTGA GGCCAAGAGT TTGAGATCAG 2970
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