| Tag | Content |
|---|
EnhancerAtlas ID | HS050-15032 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr12:11914930-11918010 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Lhx3 | MA0135.1 | chr12:11915478-11915491 | CATTAATTAATTA | - | 6.46 | | POU6F1 | MA0628.1 | chr12:11915479-11915489 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr12:11915479-11915489 | ATTAATTAAT | - | 6.02 | | ZNF263 | MA0528.1 | chr12:11915903-11915924 | ACTCTTTCTCCTTCCTCCTCC | - | 6.9 | | ZNF263 | MA0528.1 | chr12:11915909-11915930 | TCTCCTTCCTCCTCCTCCTCG | - | 7.36 | | ZNF263 | MA0528.1 | chr12:11915906-11915927 | CTTTCTCCTTCCTCCTCCTCC | - | 8.38 |
|
| | Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
| SE_01754 | chr12:11914419-11916329 | Aorta | | SE_01754 | chr12:11916394-11918023 | Aorta | | SE_09138 | chr12:11895682-11929433 | CD14 | | SE_12874 | chr12:11915526-11916313 | CD34_Primary_RO01480 | | SE_13315 | chr12:11914238-11920650 | CD34_Primary_RO01536 | | SE_14048 | chr12:11914146-11917451 | CD34_Primary_RO01549 | | SE_25354 | chr12:11914277-11930036 | DND41 | | SE_25772 | chr12:11913943-11922646 | Duodenum_Smooth_Muscle | | SE_30380 | chr12:11914693-11915878 | Fetal_Muscle | | SE_30906 | chr12:11914521-11920257 | Fetal_Thymus | | SE_32458 | chr12:11910093-11922451 | GM12878 | | SE_39367 | chr12:11914420-11925956 | Jurkat | | SE_43859 | chr12:11914295-11916262 | MM1S | | SE_43859 | chr12:11917454-11920221 | MM1S | | SE_46110 | chr12:11915046-11920204 | Osteoblasts | | SE_49833 | chr12:11914096-11919206 | RPMI-8402 | | SE_54656 | chr12:11914202-11920959 | Stomach_Smooth_Muscle | | SE_58379 | chr12:11878906-11990784 | Ly1 | | SE_58837 | chr12:11874923-11935776 | Ly3 | | SE_59849 | chr12:11874575-11943335 | Ly4 | | SE_61023 | chr12:11869475-11929777 | HBL1 | | SE_61926 | chr12:11879670-11927640 | Toledo | | SE_62748 | chr12:11877030-11934459 | Tonsil | | SE_66238 | chr12:11914420-11925956 | Jurkat |
|
| | 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 |
| GH12I011761 | chr12 | 11914429 | 11925846 |
|
Enhancer Sequence | TTCGTTTTAC CTGTGATTGT TTTGGGAGGA AGCCCTCCTG CAAGGAAATA GGGAAATCCA 60
ACACCCAGCT CTGTTGAGCA TTTCCCTATG GTTCCTGTGA TTGAAATCGG GTTAATGCTT 120
TTGTGGGATG AGAACTGGTG CCAGCTCCTA GGCCTTGCAG GGCTTCTAAA GACTGTCCCT 180
GCCACTCTTG CCTTATGCTG GTTCCCAGGA CCTTACAGCC AGATCACAGG CCTGCTCCCC 240
TGTTCTCATA GCCCCCTTTC TGGCCTGAGA ATTGTCTGTG GCTTGGCCCT TTGCCCCATG 300
CAACATGCAC AGGTGTGGCT TCTGCTAACT ATCTACTTGA CCCCAACTGT GTGATTAGCG 360
GCAATCCCCT CTGCAACTCA AGGCGTGTTT GCCTTTCCTG TAACCTGTAA AAAATTTCAG 420
TCTGCGTTTT TCTCCCTCTG GAGATGGTAT CCACTGGGTT TTAGGCTTTA CAGAGCCAGC 480
TGATCTGCGT GGATGGGCCA CACTATCCTC CCTTAGCCGG CTCCGTAGCA CATGCACAAT 540
TAATACTGCA TTAATTAATT ATGGGAGAAA AAAAGCACAG TTGGCAAGGG AATGAAGGCT 600
TTCAGCTTCT AAAGTGAAGG CTTTGATGCT GAGCTTGAAA GTACATTTCC ATCCGCCTCA 660
GCCAGCAGAG AGAATCTGTG ACACTTATAC CATCCCCTGG GCATGAAAAC TCACACCCAA 720
GGAAAGTATT TCTAAATAGA GGCCCTCAAC TAGTTGCTGG AATCATCTAC TCATTGCCAT 780
GGGCTGTGAA AAGGGGGTGT AAGATTAGGG AGAAAAGACT CGCCCAAAGC AGCAGTGATT 840
CGTGACCAAA GCTGATGAGG GGTTTTATTT TTTCTCCTTA AGTAGCTCTT AAGTCACCAA 900
CATCAGGAAC TCTTTGTAGA GAAACAAATA TGAGTAAGTG ATTTGGTGCC AGCCCTCTTG 960
AGGACATAAA ATGACTCTTT CTCCTTCCTC CTCCTCCTCG CATGCCTTGC TTCAGGAAGG 1020
AACCCTAAGG TGGTGCAGGT TCCCAAACCT GTTATTCGGA TGGGTTGGAA GGTTCATCTC 1080
TGTTAGGCAT GGTTTCCCAC TAGATATGAA CAAAGTCGGG GAGAAAATGC TTTCCTTTTT 1140
CATTCTGATT CCTTCACGCC ATTGTTCTTG AACTCCTCAG CTCCCACACT GACTCCTTTC 1200
ACTTCTCCTA TGAGGTGGTA GTGAAGCCAC CTCACAAAGT CCCCTCTCTG AACAGACGCA 1260
GTTCTCGTTC CCCTATTTAC AACTCTGTCA AGCATTTTTC GTGGGGGCTC TTGCTGACCT 1320
TAAAATTTGG CCGTGATTCA AATATTCATC CAGGTATCTG GGGTTTTATT AAAGGTCTTT 1380
TAGGAACACA AAAGTAGGAA TTCCCTGAGA GAGGTTTTCT TCACTTGAGA CTCATGGGTT 1440
ATAAATGAAA CTACTGGAAT GCCCTGACCA AGTGCTGAGA GGAGCTTCAG AGACCCACAA 1500
AAACCTAAAA AGATGTGAAA TTTGTCTCTG ATCAAATAGA TTTTGGACCT TATGAAAGAA 1560
AATAAGCTTT TCTTTTGATT CTTAGAGAAA AATTTTTGCT TCAGATGAAT CCAAGTGTGT 1620
GTGCACGCAC GTGCTTTCGT TGGGATCGTC TTATAGCTGT TATTCCAGAT ACCTGCTTCA 1680
CAAAGCTTCT GTGATTATTC CTACTACTGT GACGATTCCT GCCACCCCAG TGATCGGGGA 1740
AAAGAACTTG AAATACAACT GGGTATTGTA GCATTGGCAC TGTGCAGACG CTGTGTAGCT 1800
CTCTCATGTC TGGTACTTCT TTGTTTGCTA AAGGAGTATT GAGATTCAGA AAGTGGCTGC 1860
CTTCTAAACC TTTATTGTTC AGATAGCATT ACTTTGGACC CAGGACAGAG GGCTTATAGT 1920
TGACTGTGAA CGGGGTGAAT GTTATACTTA AGCAGGGAAT GTGGTCACCC AGTTGCAATG 1980
ATTTAGAGTG CTTTGAACAT AAATATCTCC CACGATGAAT GACCAGGGTG CCTGAAATTC 2040
CATTGTTGAG ACATTCCTTT TGGATCAGGC ATTATTTCCA CATAGCTCCA CTTTTAAAAG 2100
TAAATCATTA TGGCAGGAGA TAGTTATGGA GAGAGATAAT TAATACCTCA AGTCCCTAAT 2160
ATCTTAATGA AAATTAGCTT ATCAGATCTC CTGAATTTTT TGAAGTGGAA GGACCGTGGC 2220
CAGCACGGAG TGGGTAGAGT TGGAAATAAG CACTATAATT TGCTTAGGGC TGGCCTTCTC 2280
TGTGGATAAG ACAGATGGAA AACTAGATGG AAAATCCAGG CCTCCTGATT TAGACAAAAC 2340
ATTGTGAGCC TGGAGCTCTG AGGCCAGGAT GAGCAGTCTG CTACTTACTG TGCGTGGCCA 2400
TTGCTCTCAA GACATTGCCA TCATCAGTCT TGGCCAAAGA AGGTCAGGTC TCCTCTAGTA 2460
CACTGGCGAT TTGAGAATGT GCAAGTCATC TGCATTTCTT TGACAGGAGT AGTGAATTTG 2520
GGAGTATAAA TCTGAATCCT TAAGCCTTTC AACCATTCTC ACTAAATGTC TTTACTTCAG 2580
GGATGATCAC GTTTGATCGT AATGCCAAGA TCTTGCAGAT GTATAAAGGG CATGGTAATC 2640
CAAGTCTTGA GTTGAAGTAA GTGGTCAGGA AAATCTTGAC CCTTGGGGAA GGAGCTACCA 2700
GAGCTGGGTG GCCTATGTGT GTGTGACAGG GAGGAGGTGT GCAGAATTTG GGGGAAAGAT 2760
CCTTTGTAGT TCTCCATGTG GAATAATAAC TTCCATTTAT TGAGTGCTTA TGGTAGGCGC 2820
TTTTCACATG TATTGTATCA TTTAACCCTC TAGGCAGTCC TGTGAACTGG GTTTTATTAT 2880
CCTCATCTTA CTGATGAAGA GTCAAACTTA AAGAGGAAAA GGAACTTGAC CAGAGTCACA 2940
GAGGTGGTAG GTGGGAGACA GGTCCATCCA ATATACACCT TGCCTTCCAA TAGAAGCCAA 3000
AGCCCTATTG CCTAATCTCT TCACTTTAAG AACATGAAGA ATAGTGTTGA GTTCCCCTTT 3060
GAGATCTGAC TGTGGTTAAA 3080
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