| Tag | Content |
|---|
EnhancerAtlas ID | HS197-01348 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr1:154399370-154401670 |
Target genes | |
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 | GACTTCACCT TCTAGGGACT CAGAATTTTT TTTTTTTTTT TGAGACGGAG CTTCGCTCTT 60
TTTGCCCAGG CTGGAGTGCA GTGGCGTGAT CTCGGCTCAC TGCAAGCTCC GCCTCCCTGG 120
TTCAAGCAAT TCTCCTGCCT CAGCCTCCCA AGTAGCTGGG ATTACAGGAG CCTGCCACCA 180
CGCCCAGCAA ATTTTTTGTA TTTTTAGTAG AGACAGGGTT TCACCATGTT GGCCAGGATG 240
GTCTCGATCT CTTGACTTGT GATCCGTCTC GCCTCGGCCT CCCAAAGTGC TGGGATTACA 300
GGTGTGAGGC CCAGCTGGGA CTCAGATTTT GCTGAGGACC AGGACAGTAC TGTGTGCTGT 360
GTCCTGGCCT TGCAGCAGTG AATGTGTCTC CCGTTTCTCA AGGGCAGGTC TCTGGGATGC 420
CTGACTGTGT CTTCCTTGCC AGTGCCTGGC TGCTGCAGCC TCCTCAAATG TTTATCAAAC 480
ACAGGACTTG CCCACCGTGG GAGAAAGTAA GGCCATAGGT GTCTCAGGAA CCTGCCCAAA 540
CTCGCCTGGC TGCACGGTGA CAATTCAACC AGCTTTCTTA CCCAAGGTCT GTTGGTGACC 600
AGAGAAAACC TTAGATGACC GGCTGCCATG ATGGCCTTAT ATCTGTCCCT TTTCTGCCAG 660
CCTTGAGGTA GAGGGTGCCA GGGAGGAGGA CTCTGGCTCT AGGTGTTAAA GTGAGAGGGA 720
AGTGTGAAGG GTATCTGTAT AGCTAGACAG GGCTCAATGC CAGGCAGAGC TGTCTCCGCC 780
CCTTTGATGT CTATGTCTCT GTCCCTGGAC TGTGGCCAGT AGCCAGTGTG GACTCCAACC 840
TCACCAGCTT TAGGGGTGTT ATCTGCCTGG GAGTCACTGA TCCTTACTCC CTCCTCTGAC 900
AGCCACCTTG GATGGGGTGA AAGGAAGGAC AGCCTGCCAA GTATGAGATA AAAACGCCTC 960
ATAAACAAGA AGGGATTTGC AGGCCAGGCA GAGAGCCTTG TGCTGCTTCT GAGTCCCAGG 1020
AGCATGGGCG AGGAGGTGAG GTCAGGCACT CAGCAGCTGC TGGTCCTCTC TGAAATCTTT 1080
GGCCAGATTT ATTGCTACTG CTTGCTAATA AATGGTTATG CATTTGGTTC AAAGGACCAA 1140
GTGTGCTTAC ATGAAAACTG GCTGTGTTCC CTGGCCTCTG TTTCCTTAGC TGGTTGGACT 1200
AATTTGATTG GTTAATAAAT GAGTCCAAGG TGGTTGGGCT AATTTTTATC TTAGATTCTA 1260
TGACTCTATA ACTGCTACTC AAAAAAAGTG TACTTGTTCC TTTAATCTTT AATCTTATTT 1320
TTCTTGAGTA GTAGAATACA CCCAATTTTT TTCAAGGGGT AGAGAATGCA TTTTTTTTTT 1380
AACCTTCCAG TTTGGTCCCT AGAGTAAACA CAGCATTGCT GTAGTAGATG TAGGGTACTG 1440
GAGGGAGCAT GGAACAGGGA ACCAGAAGCC CTGGTTCCTA CCCCAGCTGG GCATCTGGGC 1500
CAGTCTCTTG ATTCCTCTGT GCCTCAGTTA CCAACTATAT AACGGGCATT CTGCCATGAA 1560
TACCCTGCGA TTTGGAAACC TCCTGTGTAC GTGTGCACTT GGGTGCCTGG CATTCATTCC 1620
TAATGGCATC CATTCGTTCA CACATTCATC CAGTACTCAG CAGACTCCTG CCATGGGCCA 1680
GGCAACGTCC CGGGCACTTG GAATATAATG GAGAACAAAG CAGGGTGCCT ACTTCTGTGG 1740
TGCTTGGAGT CTTGAGGGGA AGAGAGACAC GGAATTCGTA ATTACATGGC AGCGTGTGGG 1800
TGACGTATTG CAGAATGAGG GCCTAGTGGA GCTGGGGGAC CGGAAACGAT GTTTAGGCCG 1860
AGACCTGGAA TAGGAGGAGT TGTCGTGGGG ATGATGTAGG AAGAACGAGT GTGAGGAGGA 1920
GAGCGAGGGG AGTTGAGGGG AGGGCTCCAC ACCTTCTAAG GAGTGGGGAG AGATGAGGCC 1980
TCCAAGGACA GAAGGGCCCT GCAGGCCACG CTGAGGAGCT TGGACTTCAT CTTGTGGATG 2040
GTGGCAGGCC CTTGAAGGGT TTTCTAATCC AGGGAGTGGG GTGGCTGGAT CATGGCTTCA 2100
GAAGGCTCTC CCAGGCAGCT GGATGGTGAA GACCAGGTTG GGGAGGTCAC CAGGAGAATG 2160
CTGCCCTAAT CCAGGCAGAG GTGACGGTAG CCTGGGCCAC TTCATCATTA TCACTGAGGC 2220
CTCTCGTGGC TTCCTCAGAC CAGAACGAAG CCCCCTTCTT CAGTGGCTGT GGGCTCACCA 2280
AGTGTCTTCT CCCTCCTCCA 2300
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