| Tag | Content |
|---|
EnhancerAtlas ID | HS180-45554 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr7:104597050-104598330 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr7:104597134-104597149 | TGAACTTCTGACCTC | - | 6.38 | | RARA | MA0729.1 | chr7:104597131-104597149 | TCTTGAACTTCTGACCTC | - | 6.88 |
|
| | Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
| SE_02797 | chr7:104597100-104598363 | Astrocytes | | SE_09206 | chr7:104596230-104599708 | CD14 | | SE_10864 | chr7:104596230-104598721 | CD20 | | SE_12036 | chr7:104597035-104598349 | CD3 | | SE_14944 | chr7:104597249-104598332 | CD4_Memory_Primary_7pool | | SE_16497 | chr7:104597305-104598065 | CD4_Naive_Primary_8pool | | SE_19949 | chr7:104596740-104598426 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20140 | chr7:104596124-104598566 | CD56 | | SE_21621 | chr7:104597338-104598449 | CD8_Naive_7pool | | SE_22586 | chr7:104596522-104598442 | CD8_primiary | | SE_23243 | chr7:104597658-104598432 | Colon_Crypt_1 | | SE_23896 | chr7:104597720-104598271 | Colon_Crypt_2 | | SE_25883 | chr7:104596585-104598467 | Duodenum_Smooth_Muscle | | SE_27138 | chr7:104597660-104598437 | Esophagus | | SE_31758 | chr7:104597598-104598480 | Gastric | | SE_36016 | chr7:104596796-104598440 | HMEC | | SE_40784 | chr7:104597781-104598432 | Left_Ventricle | | SE_42639 | chr7:104597540-104598428 | Lung | | SE_43684 | chr7:104595519-104598465 | MM1S | | SE_44335 | chr7:104596231-104599334 | NHDF-Ad | | SE_44865 | chr7:104596555-104599531 | NHLF | | SE_45643 | chr7:104596366-104599440 | Osteoblasts | | SE_50161 | chr7:104596733-104598540 | Sigmoid_Colon | | SE_52521 | chr7:104596755-104598388 | Small_Intestine | | SE_54878 | chr7:104596388-104599804 | Stomach_Smooth_Muscle | | SE_56051 | chr7:104596301-104598585 | u87 | | SE_67251 | chr7:104595519-104598465 | MM1S |
|
| | 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 |
| GH07I104956 | chr7 | 104596512 | 104599449 |
|
Enhancer Sequence | AATCTAAACT TATTTCACCT TTATAAAAAT CAGTCAGGAC TATGTATTTT GGGGGCGGTC 60
TTGCTATGTT GCTCAGGCTG GTCTTGAACT TCTGACCTCA AGTGATCCTC CCACCTTGGT 120
ATCTCAAAGT GTTGAGATTA CAGGTGTGAG CCACTATGGC CACCCAGAAT CATGTGTTGT 180
ATGATTCCAC TTATATAAAA TATCCAGAAT AGGTAAATCC ACAGAGACAG AAAGCAGATT 240
AGTGGTTGGC TAGGGCCTGG GGTGTTTGGG CAGAAATAGG AACGACAGCT TTTGGGGATG 300
AGGTTTCTTT TGGGGGTGAT TAAAATGTTC TGAAGTTGTT TGTGCTGATG GTTGCACAAT 360
TTTGTGAAAC CAAATGGTAA AAACCATTGA ATTGTGCATT TTAAATGGAT GAATTGTATG 420
GAACATGAAT TGTATCTCAA TAAAGCTGTT ATTTAAAAGA AAAAAGTCAG GAATTACTCA 480
GGCGACACTG AAGAGGATGT GTACATGGCT TCTTTCCATG GAAGGAGACA AACCACCTTG 540
TATTATTGAA GAGAAAGACT CTGGTATCCC AGCCTTCTAC TCTTACTATA TACACAGTTT 600
CTATTTTGGT CCTTTTTAAA GCCTTCTTGT TATAGTTAGT GAGCAACAGT TAAGTCGAAA 660
ACCACAGTGA GGCCTTGGTT ACAGCTTACC CTTGTTTTCA ATCAACAAAA AATATGACTA 720
ATGTCACTGT GGCTCGACTC AACCACATAT GTGGATTCAG GAGGCTTTGG ACATGTGCTA 780
GAGGCTGCTG GGGCTGACCA GCTGGAAGGA CAGCAGTTAG CTGAACTTAG GCTCCAGGAA 840
TAAGATGTTG GTGAAGCCTG GGAAAATGTC TTCCGTGAGC TGGGGGTGGA AAGTTGTTGT 900
GGAAGTAACC CTGAAGGAAA AAAGAGTTCT CTGGCTGGCT TGGCCCAGAG ATACAGGCTG 960
GAAATTAGTA AGAAGAGCAG ATTTTGAGGC CAGCATTTCT CTAGCTAACT TCTAGCCCAG 1020
CGCCCCTTTT CCATCCTACT ATTTCATACA TGACCCCCAA GGGAAGCCAT ATCAGGTTCC 1080
TAGAGTTGGG AGAAGAGAGA CTCAGGGGGA ACCTGTACTG AAGTGACTGT GGCAGAGGCA 1140
GGGTGAGGCT GAAGAGCACC AGAACATGAG ACATTTCCCC GCTGTCACTT AGTAACAAGG 1200
GCCCTGTGAT GATTAATTTT ATCTGTCAAC TTGAGGGAGG CTGAGGCACA AGAATTGCTT 1260
GAGCCTGGGA GGTAGAAGTT 1280
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