| Tag | Content |
|---|
EnhancerAtlas ID | HS010-00017 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr1:12210140-12211410 |
| | 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 | ACAGAGCCCA GACTCAAGGG GAGGGGACAC AGATCCCACC CCTCATTAGG AGGAGTGTCA 60
AAGAATCTCG AGATCTTATG TGTCAGCAGG AGCACTTCAC ATACTGTCTC ATTTTAGCCT 120
CTCGGTAATT TTGCCATTAT TGTCCTTGGA GTTGGCTCAA GGAAGCTACA TAACCTGGTG 180
GAATCCCAAG TTCCTCTGGC TGGAATTTGG ATCCAAGCTG GTCTGTCTCC AGAGTGTGAG 240
CTCTGGACTG AGCAGCTGAC CTGTGCATTC AGGGACCCAT ACAGTCAGAA TGTGGCAGGA 300
CTGGAAAGCA AGCTCACATC TGTCTGATTA GAGAACATCT GAGCTTGGTA CCCATACAAA 360
CTAGGCCCTA TCTAGTTTTT AGATAGGGAA ATCAAGGCTC TGAGAGGTCT TGCCAGGCCT 420
CTCCTGAGGA AGAGGGCAGG GTCTGGGACC TTCCAGGGCA GGATGGGGCC CCCAACTTGG 480
GTTGCACAGA ACCATGTCAG GAAGTCACAT AGAGTTGTGG GTAGATTATG CAAGTACAGG 540
CTGTCAGGAG GGATGTTGTT TTTCACTGCA ATTACACTTC ACTCAGGAAA TACAGCTTCT 600
GCACGTACTG AGGGAGGGTT CCTCACCCTG TGCAGAAGAC CTCCTGGTGA ATACCGGGGC 660
ACTCGCTGGG TGACCCTGGG TCCTCTGGGC CAAGTTCATG CATCGAAAGT TCCCTGAGAA 720
GCTCTTTGTG CCCATCTGGG TTGGGCTTTG ACAATAGAGT TGAAGAGGCT TTATTCCTGC 780
CATGCATGGA GTCACAGGTT AGTAAGAAAG ATGATAAGAG CTGTACTTGA GGCTTTCGTG 840
TGCTCTCACT TAAACCTCAC AGTGCACTAG GAAGTAGTTA TTACATTACC CCTATGTTAC 900
AGATGAGGAA ACCAACACGC AGAGTGGCTA AGCCAGTTCC CCAGGGTCAC ACAGCTGCTA 960
AGTGGCGCAG CTAGGCTTTG AACCCAGGCC ACCTGGCTGG AGTCTGCGTC CTCACACACT 1020
TGGCCATGCT GCTCCATTGT GGCTCAGGCC GAGGTCACCA CTGTGCTGAG GCCCCAGCCC 1080
TGAGTCCCAG ACCCTGTAGA ACACTGTGCA GGCATCCATG GGGCTCAGTG AATGCACAGG 1140
GAATGGAATT TGCTCTTGGT TTTTATCCCA CCTTTCCTTT CCAAAGCCCA GCTGTGGCCA 1200
GGCCTCTCCC TCACAGAACC TTCTATGACT CCCTAGTGCC TACATGCCAA TGTCTGCCAA 1260
TCCAGCTTTG 1270
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