| Tag | Content |
|---|
EnhancerAtlas ID | HS117-00065 |
Organism | Homo sapiens |
Tissue/cell | LHCN-M2 |
Coordinate | chr1:16464950-16468840 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr1:16466266-16466277 | AAGCAATAAAA | + | 6.32 | | RREB1 | MA0073.1 | chr1:16467768-16467788 | CCAGGGGGGTTGGTTGGGGT | - | 6.93 | | ZNF263 | MA0528.1 | chr1:16468206-16468227 | AGAGGAGGAAGTGGGGGAAGA | + | 7.89 |
|
| | Number of super-enhancer constituents: 35 | ID | Coordinate | Tissue/cell |
| SE_01311 | chr1:16465054-16467084 | Adrenal_Gland | | SE_01311 | chr1:16467161-16468607 | Adrenal_Gland | | SE_23091 | chr1:16465053-16466236 | Colon_Crypt_1 | | SE_23091 | chr1:16466252-16467025 | Colon_Crypt_1 | | SE_23751 | chr1:16465457-16465897 | Colon_Crypt_2 | | SE_24743 | chr1:16465421-16465897 | Colon_Crypt_3 | | SE_26540 | chr1:16464423-16467134 | Esophagus | | SE_26540 | chr1:16467219-16474484 | Esophagus | | SE_29455 | chr1:16467791-16468550 | Fetal_Intestine_Large | | SE_30715 | chr1:16467395-16468971 | Fetal_Muscle | | SE_31527 | chr1:16465065-16467061 | Gastric | | SE_31527 | chr1:16467241-16474177 | Gastric | | SE_34268 | chr1:16463915-16469522 | HCT-116 | | SE_34628 | chr1:16464389-16475128 | HeLa | | SE_36144 | chr1:16465332-16467155 | HMEC | | SE_36144 | chr1:16467369-16469082 | HMEC | | SE_38062 | chr1:16464574-16469506 | HUVEC | | SE_40833 | chr1:16464800-16474529 | Left_Ventricle | | SE_42443 | chr1:16464217-16474534 | Lung | | SE_44998 | chr1:16465283-16466252 | NHLF | | SE_44998 | chr1:16466301-16467125 | NHLF | | SE_44998 | chr1:16467852-16468802 | NHLF | | SE_46140 | chr1:16464962-16469237 | Osteoblasts | | SE_47150 | chr1:16463762-16486412 | Panc1 | | SE_48744 | chr1:16464918-16474528 | Right_Atrium | | SE_52536 | chr1:16464905-16467041 | Small_Intestine | | SE_52536 | chr1:16467684-16469210 | Small_Intestine | | SE_53900 | chr1:16464743-16469386 | Spleen | | SE_56795 | chr1:16467226-16474542 | VACO_400 | | SE_64726 | chr1:16467542-16468812 | NHEK | | SE_65472 | chr1:16465146-16466178 | Pancreatic_islets | | SE_65472 | chr1:16466192-16467043 | Pancreatic_islets | | SE_65472 | chr1:16467559-16468683 | Pancreatic_islets | | SE_69141 | chr1:16464511-16467047 | H9 | | SE_69141 | chr1:16467939-16468895 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 16467375 | 16467979 | | chr1 | 16465200 | 16468800 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I016137 | chr1 | 16464252 | 16469121 |
|
Enhancer Sequence | ACAAGGACAT CAGTTCAATC TGCTTCCACC CCACGTGACT GTCTCATTCC CTCACCAGGG 60
ACCCCTGCCC TGCAAGCAGG TCAGTAAATC TCTATGGACC TGTTTTCTCA TCGGCAAAAT 120
GTCTTGTGAT GGAAAAATGC ATGGCAAGGG CCTAGCATGT ACCGGGCACC CAGGAAGTGC 180
TTCACACACA TGCTGCAAAC CTTTGCTTCA CTCCCCACTG GCTCCTGCAA GAAGCACCAC 240
GCCCCTGAGC CTGGCATTCA AGGCCATACC TCGCCTTTCA GCCAACCAAG AATCCCATCA 300
CAGCCTAGCT CAGCACTTGA CCAAGCACGC TGCCCACCGG CCTCATCCCC TTTCCTCCAT 360
GCAGACTAGC CTGTCCGGTC CCCACCTGGG TAGCTGAGAG CTGCCCAGGG CAATGACTGC 420
CTCTTCTTGA CCATGTGTGT TTGTTGACTG TCACCACCAC CCTGACTCAC TGGCCAGCCT 480
CATCAGTTCA GGATGCCATC CCTGCAGGTG TTACCTCCAG CCCAGGACCT GCCCTCCTTT 540
CCATCCGGGG CTGACCAGGA AGCAGGAAAG GCCAAGCCCC CTGGCATTTT CTCTGGCTCT 600
GCTTCCAGGA CCGAGTCATA TCCGCCACTC ACAAGGACAG CCAGGAAGTG ACTCTTCCTC 660
CCCCAGTGGC CAGTCCTGTC CTGGCCCAGC AGGCTGGGGG CTCAGGCACC TGACTCCGGG 720
GGCTTCTTCC TCCCACCGCC CTATCCTGTC TCATCCCGCC CCTGCCCTAA GCCCCTTCCT 780
GGCCCTACAG GCAGGAAGCT GCCCAGACAC AGGGCTCACG GTGCAGGGCT GTCCAGGGCT 840
TGGGCAGCTG CTGAAGTGGC CAGGGTGGGT AGAGGTCACC CTAGGGAGCT CCTCCAACAA 900
CCCTACAATT ATAATCCTTC AGATTGTTCT GATGAGAGGG TCCTGAGACA CCTCCAACCT 960
CAGCACCGTG TTCACCACAC ACACAATGAT CCTCTGCTCT GTGCCTGGCC CACCCCCAGT 1020
GCTGGGTATG CACCAAGATG AAAACAAACT CCTGATCTCA GGGAGCAGAA GCACCTGACA 1080
AGGTCTGCAA GACAGAGGGA GGAAACAAGC TAACAGCTAA GGGGGTGGAG AAGGGGAAAC 1140
AACCTTGGCC AGGAGTCTGA GAAGTCACAG AGGGGACATT TTGGCTGGGG TTCAGAGGCT 1200
GCATAGGAGT TCAGCAGGGG AATGATAGAT GTTGGGAGAG GGAGTTAGGA GTGAGAAAGT 1260
GCATGACTAA TACGGAAGGT ATGAGTGGGT TTGTGGGCAC AAATGTGGGG AGCAGCAAGC 1320
AATAAAACAG TTGAGAAAGG CCTTCAATGC CAGGCCAAGA AGCTGGGACT TTATCCTGGA 1380
GGCAATGGAA AGCCGCTGGA GGTCTGATGT GGAGAAGTCA GACCCCTGCC GTCAGGAAAA 1440
ATCTGTGCCT GGAGGCAGCT TTTGTCCAAG ACCCTGGGGA CAACCTGGCC CCTAATGGCC 1500
TAAGGACAAC CCCCTCCAGG GAAGCAATTT CAAGTGCCCT GACCCAAGCA AACCTGCTAA 1560
CTCTCAGGGA CAGAATCTGG AGCGAAGACT CTCGTCATCC AGTCCCCTGT GTGAGCAGAG 1620
GTGCAGAGGG GGACCAGGAG TCAGGGGAAC AGGACTCAAA GGACACCCAG CTCTGTAAGG 1680
TGCCAGATAG TGACCTCCTG CTGATGACTC TGCTCTCAGA GCCAGGCTGC ATCCCTGTCC 1740
CCTCCCAACC CTGGCCCAGG GACCACACAA ACAGCCGCTC TCACCCCCTT GGTCCATCCT 1800
GCTTCTGCAG ACCCTCAGCA TTGGCCCTGC AAGAGCTCAG GCACATAGGG CAGGGAAGGG 1860
GGCTTGTCCC AGGTCATGCA GCAGGACAGA GGAGGCCCGG GACCCGACTC CTGCTCTGCA 1920
CAGAGCCTGG AGTCCCAATG ACAGTACCTA CTATGCGCAG GGCTCGGGCT AAGCACTGTA 1980
CCCTCATTTA GTCCTCGCAA TAGACCTGCT ATATACAGGC ACTATTAGCG CTGGTTCCAC 2040
TTTGGAGGTG AGGAGAGACA AAAAAGCTTG TCCAAGGTCA CCAAGCTCCC AAGAAGGAAA 2100
CCAGAACTCA AACTTAGGAT GCCTGATTTT CAGCCTCTCT CCTCTCCCAC TCCTTTTTCA 2160
TTATTTATTT ATTTTGTTTT TGAGATGGAG TCTCGCTCTG TTGCCCAGGC TGGAGTGAAG 2220
TGGTGGGATC TCAGCTCACT GCAACCTCCG CCTCCTGGGT TCAAGCAATT CTCCTGCCTC 2280
AGCCTCCTGA GTAGCTGGAA CTACAGGCAC CGGCCATCAA GCCTGGCTAA CTTTTGTATT 2340
TTTAGTAGAG ATGCAGCCTG GTCTCGAACT CCTGGCCTCA AGTGATCCAC CCGTCTCGGC 2400
CTCCCAAAGT GCTGGGATTA CAGGCGTGAG CCACCGCGTC CGGCCTATTT TATTTTTTAG 2460
AGACGGGGTG TGTCTTTGTT GCCCAGGCTG GTCTCTTGAC CTCCTGGCCT CAAGTGATCC 2520
TCCCACCTCG ACTTCCCACA ATGCTGGGAT TACAGGCGTG AGCCACCTCA CCGGGCCTCC 2580
TTTCCCACTT CTGTTCTTAG GAACACTTCA ATTTGGAGCA AAGATAAATC AACATTCTGA 2640
AACAAGCCTG AAGAGAGAGG AGATAAGGCC TGACCCACTT CAAAAGCCAG AAACTCCTGA 2700
CGAATTTCAG AGCAGCTGTG GGTCTATGTG TTGTGGAGGA GGGGAGGGTA TTCCCCACCA 2760
CAGATCTTCT CAAACTGGGC ACTTTTGTGT CTGTGAGCAG AAAAGTGTAG ACTCCAGCCC 2820
AGGGGGGTTG GTTGGGGTGG CTGAAGTGGT CTCCTTCAAG CCCCGAATGT CTTCAAGTCT 2880
CCTATTGTAT TTGGAAACCC ATGAGTATAT TGCATCCCTC CCCATAACAT ATCTGCATGA 2940
TACAAAAATA GCTCTCTCCT CCACCAGATC TGTGAGTAAA ACTGAGACTC CAGAAAGCTG 3000
GGCCATGTTT ATCCTGGGGT CAGTTCCCCC AAATGCCCTG ACTTGTCTGT GGAGGAGACT 3060
TCACCTGGCT CAGTGCTGGT TCAGGTGGTC CAGGGCCAGC TGACTTGGGA AGCTCGGGGG 3120
CGTTCCCAGC CCAGGCTCTC AGGCCAGGCA GGGGCCATAA ACCCCCACAG CCCAGGCTCG 3180
GACCCACTGG AGGCTTTAGC CACCTGCAAA CCCTCACAAT GCCCCGACTC CCCACCGTGT 3240
GGCTGCTTCT ATGCCAAGAG GAGGAAGTGG GGGAAGAGAT GGGCTCTTTG GCCCCAGCGC 3300
CCGGGGGTGG CCTGCCTGCC TGCTGCCGCC AGGAAAGAGG GAATTTGGAG AGATTTCCGC 3360
TGCGGATGTG CCAGATAATA CAGCAGAGAG GCAGCGTCAA CAGGGCATGT GCCTGCCTGA 3420
CGAGATGTGC TTCCCCTCCT CCAACCACAA AGCTACCAGG GGCTGTCTCC AGGGCCCCGC 3480
CAGAGTTTCC AAGTGCTCAG GGGTCCCAGA GTTCATGAGT AGGACACCAG CAAGCCCCTG 3540
TGTTCTTCCT GACTTTATCT AGTTGGATTT CCTGGCATTC TAGGCGGGCA AGTGGGGACA 3600
GGGGTCACAC ACACTCAAAC ACACCCACAT ACACCAGATA CCTACTGTTC CTTAGCCAAC 3660
CAGCAAACTC CTATGCATCC TTTAATACCC AGCTTAAGCT CCTCTACACA GCCCTCCCAG 3720
ACTGCCCAAT TCCTGGCCCC CCGGCCCCCA TTAGGGCATC TATTAATCTT ATGTTTACCA 3780
AATAGAAATG GGCACTTCAT ACGTGTCTGG CACAATGCTG GGTGCTAGGA TGCGATGGTG 3840
AGACAGATAA ACACTGTTTC AGCTCCAGGG GAATTCAAAA CTTGGCTTTT 3890
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