| Tag | Content |
|---|
EnhancerAtlas ID | HS129-02207 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:154399290-154401670 |
Target genes | | Number: 14 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF7L2 | MA0523.1 | chr1:154400148-154400162 | CCCCTTTGATGTCT | - | 6.14 | | ZNF263 | MA0528.1 | chr1:154401281-154401302 | TGAGGAGGAGAGCGAGGGGAG | + | 6.42 |
|
| | Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
| SE_00437 | chr1:154399481-154401751 | Adipose_Nuclei | | SE_01040 | chr1:154399528-154400582 | Adrenal_Gland | | SE_01040 | chr1:154400681-154401626 | Adrenal_Gland | | SE_06653 | chr1:154399347-154403450 | Brain_Hippocampus_Middle | | SE_09189 | chr1:154398672-154408855 | CD14 | | SE_16173 | chr1:154399945-154400671 | CD4_Naive_Primary_7pool | | SE_18405 | chr1:154399517-154407766 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19165 | chr1:154401205-154402489 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_24531 | chr1:154399580-154400359 | Colon_Crypt_2 | | SE_26130 | chr1:154399302-154401704 | Duodenum_Smooth_Muscle | | SE_26877 | chr1:154399516-154400662 | Esophagus | | SE_26877 | chr1:154400694-154402391 | Esophagus | | SE_32086 | chr1:154399571-154400607 | Gastric | | SE_32086 | chr1:154400656-154401897 | Gastric | | SE_41139 | chr1:154399325-154402156 | Left_Ventricle | | SE_41647 | chr1:154399531-154400535 | LNCaP | | SE_41647 | chr1:154400745-154403911 | LNCaP | | SE_42431 | chr1:154399355-154400656 | Lung | | SE_42431 | chr1:154400696-154402137 | Lung | | SE_47983 | chr1:154399591-154400258 | Pancreas | | SE_47983 | chr1:154400922-154401243 | Pancreas | | SE_48261 | chr1:154399318-154401864 | Psoas_Muscle | | SE_48934 | chr1:154399344-154402194 | Right_Atrium | | SE_50453 | chr1:154399516-154401315 | Sigmoid_Colon | | SE_51380 | chr1:154399138-154401914 | Skeletal_Muscle | | SE_52880 | chr1:154399518-154401631 | Small_Intestine | | SE_54618 | chr1:154399097-154409137 | Stomach_Smooth_Muscle | | SE_62668 | chr1:154357227-154415486 | Tonsil | | SE_65390 | chr1:154399323-154400849 | Pancreatic_islets | | SE_65390 | chr1:154400868-154402476 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 154399696 | 154400530 | | chr1 | 154399716 | 154400696 | | chr1 | 154400830 | 154400990 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I154427 | chr1 | 154399576 | 154401508 |
|
Enhancer Sequence | AGCTATACTG TAGTTGTGGC TTTTTATAAC CCTTTCAAGC CCTCTGGGCA GTAGCAGTCC 60
ACCCCTTATT GCCCTCAGTG GACTTCACCT TCTAGGGACT CAGAATTTTT TTTTTTTTTT 120
TGAGACGGAG CTTCGCTCTT TTTGCCCAGG CTGGAGTGCA GTGGCGTGAT CTCGGCTCAC 180
TGCAAGCTCC GCCTCCCTGG TTCAAGCAAT TCTCCTGCCT CAGCCTCCCA AGTAGCTGGG 240
ATTACAGGAG CCTGCCACCA CGCCCAGCAA ATTTTTTGTA TTTTTAGTAG AGACAGGGTT 300
TCACCATGTT GGCCAGGATG GTCTCGATCT CTTGACTTGT GATCCGTCTC GCCTCGGCCT 360
CCCAAAGTGC TGGGATTACA GGTGTGAGGC CCAGCTGGGA CTCAGATTTT GCTGAGGACC 420
AGGACAGTAC TGTGTGCTGT GTCCTGGCCT TGCAGCAGTG AATGTGTCTC CCGTTTCTCA 480
AGGGCAGGTC TCTGGGATGC CTGACTGTGT CTTCCTTGCC AGTGCCTGGC TGCTGCAGCC 540
TCCTCAAATG TTTATCAAAC ACAGGACTTG CCCACCGTGG GAGAAAGTAA GGCCATAGGT 600
GTCTCAGGAA CCTGCCCAAA CTCGCCTGGC TGCACGGTGA CAATTCAACC AGCTTTCTTA 660
CCCAAGGTCT GTTGGTGACC AGAGAAAACC TTAGATGACC GGCTGCCATG ATGGCCTTAT 720
ATCTGTCCCT TTTCTGCCAG CCTTGAGGTA GAGGGTGCCA GGGAGGAGGA CTCTGGCTCT 780
AGGTGTTAAA GTGAGAGGGA AGTGTGAAGG GTATCTGTAT AGCTAGACAG GGCTCAATGC 840
CAGGCAGAGC TGTCTCCGCC CCTTTGATGT CTATGTCTCT GTCCCTGGAC TGTGGCCAGT 900
AGCCAGTGTG GACTCCAACC TCACCAGCTT TAGGGGTGTT ATCTGCCTGG GAGTCACTGA 960
TCCTTACTCC CTCCTCTGAC AGCCACCTTG GATGGGGTGA AAGGAAGGAC AGCCTGCCAA 1020
GTATGAGATA AAAACGCCTC ATAAACAAGA AGGGATTTGC AGGCCAGGCA GAGAGCCTTG 1080
TGCTGCTTCT GAGTCCCAGG AGCATGGGCG AGGAGGTGAG GTCAGGCACT CAGCAGCTGC 1140
TGGTCCTCTC TGAAATCTTT GGCCAGATTT ATTGCTACTG CTTGCTAATA AATGGTTATG 1200
CATTTGGTTC AAAGGACCAA GTGTGCTTAC ATGAAAACTG GCTGTGTTCC CTGGCCTCTG 1260
TTTCCTTAGC TGGTTGGACT AATTTGATTG GTTAATAAAT GAGTCCAAGG TGGTTGGGCT 1320
AATTTTTATC TTAGATTCTA TGACTCTATA ACTGCTACTC AAAAAAAGTG TACTTGTTCC 1380
TTTAATCTTT AATCTTATTT TTCTTGAGTA GTAGAATACA CCCAATTTTT TTCAAGGGGT 1440
AGAGAATGCA TTTTTTTTTT AACCTTCCAG TTTGGTCCCT AGAGTAAACA CAGCATTGCT 1500
GTAGTAGATG TAGGGTACTG GAGGGAGCAT GGAACAGGGA ACCAGAAGCC CTGGTTCCTA 1560
CCCCAGCTGG GCATCTGGGC CAGTCTCTTG ATTCCTCTGT GCCTCAGTTA CCAACTATAT 1620
AACGGGCATT CTGCCATGAA TACCCTGCGA TTTGGAAACC TCCTGTGTAC GTGTGCACTT 1680
GGGTGCCTGG CATTCATTCC TAATGGCATC CATTCGTTCA CACATTCATC CAGTACTCAG 1740
CAGACTCCTG CCATGGGCCA GGCAACGTCC CGGGCACTTG GAATATAATG GAGAACAAAG 1800
CAGGGTGCCT ACTTCTGTGG TGCTTGGAGT CTTGAGGGGA AGAGAGACAC GGAATTCGTA 1860
ATTACATGGC AGCGTGTGGG TGACGTATTG CAGAATGAGG GCCTAGTGGA GCTGGGGGAC 1920
CGGAAACGAT GTTTAGGCCG AGACCTGGAA TAGGAGGAGT TGTCGTGGGG ATGATGTAGG 1980
AAGAACGAGT GTGAGGAGGA GAGCGAGGGG AGTTGAGGGG AGGGCTCCAC ACCTTCTAAG 2040
GAGTGGGGAG AGATGAGGCC TCCAAGGACA GAAGGGCCCT GCAGGCCACG CTGAGGAGCT 2100
TGGACTTCAT CTTGTGGATG GTGGCAGGCC CTTGAAGGGT TTTCTAATCC AGGGAGTGGG 2160
GTGGCTGGAT CATGGCTTCA GAAGGCTCTC CCAGGCAGCT GGATGGTGAA GACCAGGTTG 2220
GGGAGGTCAC CAGGAGAATG CTGCCCTAAT CCAGGCAGAG GTGACGGTAG CCTGGGCCAC 2280
TTCATCATTA TCACTGAGGC CTCTCGTGGC TTCCTCAGAC CAGAACGAAG CCCCCTTCTT 2340
CAGTGGCTGT GGGCTCACCA AGTGTCTTCT CCCTCCTCCA 2380
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