| Tag | Content |
|---|
EnhancerAtlas ID | HS182-06313 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr14:55573560-55575770 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr14:55575108-55575119 | GATGAGTCACC | - | 6.32 | | JUND | MA0491.1 | chr14:55575108-55575119 | GATGAGTCACC | - | 6.62 | | ZNF263 | MA0528.1 | chr14:55575036-55575057 | GGAGGAGGGCGAGGGGAGAGG | + | 7.74 |
|
| | Number of super-enhancer constituents: 32 | 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 | chr14:55574297-55574562 | Colon_Crypt_2 | | 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 | AACTTAAATG TAGATTCATA AATTATTTCT TTTGTGTTTT TATCTTTTAT TGTTTTTTGA 60
GACAGAGTCT CACTCTGTTG CCCAGGCTGG AGTACAGTGG CTTGATCTCG GCTCACTACA 120
ACCTCCACCT CCTGGTTCAA GTGATTGTCC TGTCTCACCC TCCCCAGTAA CTGGGATTAC 180
AGGCGCCCAC CACCACACCC AGGTAATTCT TGTGTTTTTG TAGAGGTGGG GTCTCGCCAT 240
GTTGTCCAGG CCGGTCTGGA ACTCCTGGCC TCAAGCGATC TGCCCGCCTC AGCCTCCCAA 300
AGTGCTGGGG TTACAGGCGT GAGCCACTGC GCCCGGCCTC CTTGGTATTT TTATGTCTAT 360
TTTTTTAGAT GGAGTCTCGC TCTGTCCCCC AGGCTGGAGT GCAGTGGCGC GATCAGCTCA 420
CTGCAACCTC CACCTCGCGG GTTCAAGCAA TTCTCCTGCC TCAGCCTCCT GAGTAGCTGG 480
GATTACAGAC GTCCATCAAC ACGCCCAGCT AATTTTTGTA TTTTTAGTAG AGATAGGGTT 540
TCACCATGTT GGCCAGGCTG GTCTTGAACT GCCTACCTCA GGTGATCCAC CCACCTTGGC 600
CTCCCAAAGT GCTGGGATTA CAGGCGTAAG CCACCTGCGC CTGGCCGGTA TTTTTAAATT 660
AGAGTTCTTC TAAGATTTAT CTGAAAAAGT TACACTACTA AAAAATTTGC AACCCACACC 720
CAAGGACATA ATTTGTCTGG GCATAGAGAC TTGATGGCAC TTCAAGTAGC TGGATGAGCT 780
TCTCTTAACA TGCGATTTCT CTCAGGTTTA CATTCTTCTT GACTGCCCTT GTTCCTTTCC 840
TATTCTATTT GAAGCAAAAT GGTTAACGTT CTTCCACTTT CACCAGGACA GCCCTATTTG 900
CCCCTTCCTT GTCCTTGTTA GCCTGGTTTT ATAAAGCCTC TTTTGCAGGG GTCGGAACAG 960
TTAATAGCAT TGGGGATTGT CGCTTGTTCC CTGTAGATGA AAAGTATTTT TCTATTGTTT 1020
AAAAAAAAAT CGAGGTCATT CTCCAAAGTA ATTTCCTGAA ATAAAGCGTG GGAGGAAGTC 1080
ATGGGCATGA GGATGAGTCA TCAGGCAGCA GCACGAGGCT GCAGGCGTGA GCTGGGGAGC 1140
CCTGGCTCAG TCCTCCGCAG GCTTGGATCC CTGAGCGGAG CAGGCCACTG GGGCCTTCTG 1200
CCGTGAGAAG AGACCTACTG AGAGGCGGGG AGTGGGGGTG GGAGTGGTTG CTTCTGACCT 1260
GTAGGACAGT GGTCAGCGTG GGCGGGTGGA GGCACAGGAG AAGGCCGACA GGCCCTGGGT 1320
CCTAGGGCCA CTCAGCTGCT GGAAAATGAA GTTCAGAGTT GTTTGGACTG TCTGAAGTAG 1380
GATAGAACCA GCCTTAGCCC TAGTTAGGTA ACACATGGCA GAGGCACCTG AGCAAAGACG 1440
TGAGCTGGAC CATGGGCTTC CTGGCAGGAC TTCCACGGAG GAGGGCGAGG GGAGAGGAGC 1500
AAGGGAGCAG AAGGCAGCTT GCCGTCCACG AAGCCTCCTG AGGCCCCAGA TGAGTCACCA 1560
GACAACAGCC TGTCTACTTA AAGCAACTGC TGGGCAACTG CTGAGTAGAA CAGTCCCTAA 1620
CCACATGAAC ACTGGGGAGG AGGTTCTGAA AGACGCTGCT GGGTGCAAGG TCCCTAACTA 1680
GGGTAATCCA ATTTCACTCC AGGCTAACAT GAGAAATTAT GACTCCAGCA GCCAATCCTG 1740
TGGGCCGTGA GAGAGTGGGA GAGGGATTTT CCAGATATAA GTCCCACTAG AGCTTCTTTT 1800
TTTTTTTTTT TTTTGATACG GAGTCTCACT CTGTTATCCA CGCTGGAGTG CAGTGGCACC 1860
ATCTCGGCTC ACTGCAAGCT CCGCCTCCCG GGTTCAAGCG ATTCTGTTGC CCCAGCCTCC 1920
TGAGCAGATG GGACTACAGA TGTGCACCAC CATGCCCAGC TAATTTTTGT ATTTTTAGTA 1980
GAGACAGGGT TTCACTATGT CGGCCAGGCT GGTCTCGAAC TCCTGACCTC ATGATTCTCC 2040
TGCCTTGGCC TCCTAAAGTG TTGGGATCAC TGGCATAAGC CACAGCTTCC GGCTGAGTCC 2100
CACTAGAGCT TCTAAGAAGA AATTAGGGAA GCAGGATTAT GAGAGGCCTG GTCCCACTCA 2160
CAGTGTGCGA CATCACTGAT GACTATGCTT GGTTACCTGC CTTGTTATTT 2210
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