| Tag | Content |
|---|
EnhancerAtlas ID | HS048-00304 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:12209850-12211380 |
| | Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
| SE_00369 | chr1:12202440-12211059 | Adipose_Nuclei | | SE_04546 | chr1:12209905-12211237 | Brain_Anterior_Caudate | | SE_06521 | chr1:12209695-12211557 | Brain_Hippocampus_Middle | | SE_09154 | chr1:12199965-12214486 | CD14 | | SE_10696 | chr1:12207898-12214373 | CD19_Primary | | SE_11902 | chr1:12208865-12214231 | CD3 | | SE_14553 | chr1:12208809-12214332 | CD4_Memory_Primary_7pool | | SE_15480 | chr1:12208768-12214030 | CD4_Memory_Primary_8pool | | SE_16369 | chr1:12209491-12212458 | CD4_Naive_Primary_8pool | | SE_16946 | chr1:12210087-12214122 | CD4p_CD225int_CD127p_Tmem | | SE_17650 | chr1:12208923-12214185 | CD4p_CD25-_CD45RAp_Naive | | SE_17827 | chr1:12206501-12214454 | CD4p_CD25-_CD45ROp_Memory | | SE_18389 | chr1:12206868-12214379 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19117 | chr1:12208827-12214340 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20048 | chr1:12207907-12214477 | CD56 | | SE_20873 | chr1:12208284-12214108 | CD8_Memory_7pool | | SE_22347 | chr1:12207903-12214404 | CD8_primiary | | SE_26251 | chr1:12206411-12213727 | Duodenum_Smooth_Muscle | | SE_27503 | chr1:12209763-12212109 | Esophagus | | SE_30788 | chr1:12209786-12211445 | Fetal_Muscle | | SE_32030 | chr1:12209823-12210827 | Gastric | | SE_32030 | chr1:12210903-12211697 | Gastric | | SE_41498 | chr1:12209754-12211519 | Left_Ventricle | | SE_42336 | chr1:12209781-12214078 | Lung | | SE_48967 | chr1:12209749-12211554 | Right_Atrium | | SE_50250 | chr1:12207958-12214180 | Sigmoid_Colon | | SE_52522 | chr1:12206320-12214007 | Small_Intestine | | SE_53313 | chr1:12206186-12214442 | Spleen | | SE_55394 | chr1:12209790-12211650 | Thymus | | SE_59216 | chr1:12197780-12224862 | Ly3 | | SE_61096 | chr1:12184746-12245090 | HBL1 |
|
| | 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 |
| GH01I012140 | chr1 | 12200161 | 12214656 |
|
Enhancer Sequence | TTTGCTCACA AATCTGCAAT GTGGCCTGGA CTTAGCAGGG GAGGTGCATC TCGGCTCACA 60
TAGTACCAGC GGGGGTGATG AGATGAGCTG GAGAATCCAC CTCCAAGAGG GCTGGCAAAT 120
TGGTACTGGC TGTCAGTTTC TCTCTGTGGA GCTTCTTGGG CTTCCTCACA GCATGGCTGC 180
TGGGTTCCTG GAGCCAACAA CTCCGGGGGC AGGAAGTAGA AACTGCCAGC GTCATAAAAT 240
TTGACCCCGG AAACTGGCAC TGCATCCCCT TTGCTGCATT CCAGGTAGTC ACAGAGCCCA 300
GACTCAAGGG GAGGGGACAC AGATCCCACC CCTCATTAGG AGGAGTGTCA AAGAATCTCG 360
AGATCTTATG TGTCAGCAGG AGCACTTCAC ATACTGTCTC ATTTTAGCCT CTCGGTAATT 420
TTGCCATTAT TGTCCTTGGA GTTGGCTCAA GGAAGCTACA TAACCTGGTG GAATCCCAAG 480
TTCCTCTGGC TGGAATTTGG ATCCAAGCTG GTCTGTCTCC AGAGTGTGAG CTCTGGACTG 540
AGCAGCTGAC CTGTGCATTC AGGGACCCAT ACAGTCAGAA TGTGGCAGGA CTGGAAAGCA 600
AGCTCACATC TGTCTGATTA GAGAACATCT GAGCTTGGTA CCCATACAAA CTAGGCCCTA 660
TCTAGTTTTT AGATAGGGAA ATCAAGGCTC TGAGAGGTCT TGCCAGGCCT CTCCTGAGGA 720
AGAGGGCAGG GTCTGGGACC TTCCAGGGCA GGATGGGGCC CCCAACTTGG GTTGCACAGA 780
ACCATGTCAG GAAGTCACAT AGAGTTGTGG GTAGATTATG CAAGTACAGG CTGTCAGGAG 840
GGATGTTGTT TTTCACTGCA ATTACACTTC ACTCAGGAAA TACAGCTTCT GCACGTACTG 900
AGGGAGGGTT CCTCACCCTG TGCAGAAGAC CTCCTGGTGA ATACCGGGGC ACTCGCTGGG 960
TGACCCTGGG TCCTCTGGGC CAAGTTCATG CATCGAAAGT TCCCTGAGAA GCTCTTTGTG 1020
CCCATCTGGG TTGGGCTTTG ACAATAGAGT TGAAGAGGCT TTATTCCTGC CATGCATGGA 1080
GTCACAGGTT AGTAAGAAAG ATGATAAGAG CTGTACTTGA GGCTTTCGTG TGCTCTCACT 1140
TAAACCTCAC AGTGCACTAG GAAGTAGTTA TTACATTACC CCTATGTTAC AGATGAGGAA 1200
ACCAACACGC AGAGTGGCTA AGCCAGTTCC CCAGGGTCAC ACAGCTGCTA AGTGGCGCAG 1260
CTAGGCTTTG AACCCAGGCC ACCTGGCTGG AGTCTGCGTC CTCACACACT TGGCCATGCT 1320
GCTCCATTGT GGCTCAGGCC GAGGTCACCA CTGTGCTGAG GCCCCAGCCC TGAGTCCCAG 1380
ACCCTGTAGA ACACTGTGCA GGCATCCATG GGGCTCAGTG AATGCACAGG GAATGGAATT 1440
TGCTCTTGGT TTTTATCCCA CCTTTCCTTT CCAAAGCCCA GCTGTGGCCA GGCCTCTCCC 1500
TCACAGAACC TTCTATGACT CCCTAGTGCC 1530
|
