EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS050-01751 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr1:36830810-36833160 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:36831989-36832007GCTGCCTCCCTTCCTGCC-6.32
Myod1MA0499.1chr1:36831814-36831827GGGAGCAGCTGCA-6
Nr2f6(var.2)MA0728.1chr1:36832667-36832682TGAACTCCTGACCTT-6.04
ZNF263MA0528.1chr1:36832136-36832157CCTTTCCCTGCCCCATCCTCC-6
ZfxMA0146.2chr1:36830834-36830848CCCGCCTCGGCCTC+6.01
Number of super-enhancer constituents: 47             
IDCoordinateTissue/cell
SE_00264chr1:36830417-36836190Adipose_Nuclei
SE_01346chr1:36831434-36832235Adrenal_Gland
SE_03711chr1:36831036-36831843Brain_Angular_Gyrus
SE_04744chr1:36830783-36832569Brain_Anterior_Caudate
SE_06364chr1:36830459-36833894Brain_Hippocampus_Middle
SE_07553chr1:36830450-36832653Brain_Hippocampus_Middle_150
SE_08563chr1:36830458-36833774Brain_Inferior_Temporal_Lobe
SE_09252chr1:36830385-36842613CD14
SE_10618chr1:36830718-36832499CD19_Primary
SE_11159chr1:36829411-36836756CD20
SE_13460chr1:36830712-36832055CD34_Primary_RO01536
SE_13460chr1:36832637-36833702CD34_Primary_RO01536
SE_14329chr1:36831560-36832119CD34_Primary_RO01549
SE_14627chr1:36830548-36833802CD4_Memory_Primary_7pool
SE_18215chr1:36830641-36835788CD4p_CD25-_CD45ROp_Memory
SE_18903chr1:36830547-36835076CD4p_CD25-_Il17-_PMAstim_Th
SE_19575chr1:36830747-36832588CD4p_CD25-_Il17p_PMAstim_Th17
SE_19575chr1:36832620-36833928CD4p_CD25-_Il17p_PMAstim_Th17
SE_20413chr1:36831217-36832269CD56
SE_20930chr1:36831029-36832539CD8_Memory_7pool
SE_24109chr1:36831573-36831990Colon_Crypt_2
SE_26702chr1:36830809-36832597Esophagus
SE_27925chr1:36830993-36832311Fetal_Intestine
SE_28867chr1:36831174-36832322Fetal_Intestine_Large
SE_30355chr1:36830737-36832474Fetal_Muscle
SE_31812chr1:36831426-36832433Gastric
SE_31812chr1:36832734-36833261Gastric
SE_37159chr1:36830252-36833579HSMMtube
SE_38175chr1:36831448-36833647HUVEC
SE_41385chr1:36831174-36832572Left_Ventricle
SE_41942chr1:36831495-36832017LNCaP
SE_41942chr1:36832662-36833800LNCaP
SE_44847chr1:36830916-36832317NHLF
SE_45845chr1:36830713-36832599Osteoblasts
SE_45845chr1:36832743-36833692Osteoblasts
SE_48926chr1:36831440-36832524Right_Atrium
SE_50223chr1:36830762-36832480Sigmoid_Colon
SE_50223chr1:36832626-36833748Sigmoid_Colon
SE_51487chr1:36830771-36832480Skeletal_Muscle
SE_51965chr1:36830920-36832423Skeletal_Muscle_Myoblast
SE_52539chr1:36830812-36832545Small_Intestine
SE_55982chr1:36830938-36832564u87
SE_62579chr1:36814176-36867515Tonsil
SE_63764chr1:36830802-36832494HSMM
SE_65601chr1:36831447-36832451Pancreatic_islets
SE_65601chr1:36832550-36833219Pancreatic_islets
SE_67689chr1:36830938-36832564u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr13683114636831500
chr13683160036832200
chr13683307636833152
Number: 1             
IDChromosomeStartEnd
GH01I036365chr13683073736836194
Enhancer Sequence
GAACTCCCGA CCTCAGGCGA TACGCCCGCC TCGGCCTCCC AAAGTGTTGG GATTACAGGC 60
ATGAGCACCG CGCCCGGCCT GTTTTGGCCC TTATTCTAAA CCCTAGGAGA CTGACTATAT 120
GTGGTGCACC AGAAAGTAAG AGGGATGATC CATTGCACTG CAGGTCTAAT CTACCAGGCT 180
CCCAATTTGT TTTCAGAGCT GTGCCACTGG GGAGCACAGC CATGACTTAA TTTTGAGAAT 240
AACTAGGATT GTGTAACTCA CTGAGCCCCA ACAGTCCCCA GATGGAGCAG AAGCCACAGT 300
TAGGCTTGGC TGGGCCTTCT GCCAAAGAGG CTCATGCTGG AAGCAGATTC AGTGTCATTC 360
ACATAAAAGC AGAGAAGGGT AAAACTGCTT CTAGAAATAT CTTTAAAAGC TGGGCAGTAA 420
TGTGTCTGGC ACTGTGTTCC TGCTCTTTGC TTGCCTAACT CCTACGCATC CTTCTCAATC 480
TAAGTATCAC TTCCTCAGAG AAGTCTTCCT TGATAACCTC ATGACCAGTG GGTCCCAGTT 540
AGTCTCACTC ATGGTGGTCT GTAATTTTCC TCCATAGTAC TTTCCAGATT TTGTAACTAT 600
GTATTTATTT GTGTTTATAT GCTTAATGTC TGCCCCCCTC CACCAGAAAA ATTCCACCAC 660
AACTAAAAAT TTCACAAGGA AAAACAAATG TATAAACATA TATATAAAAC CACTGCAGCC 720
CACTGCCAGG CCCAGCAGAT ACTCCATGAG TGAACGGATA CCTTCCCTCC AGCTGGTGAC 780
AGTCATTGCC AGGGTCGGCG GCCCTGGGCC TGTCCTGCGC TGCCCACTGC CTCCAATAGT 840
AAGTTGGTAT CACCACCCTT CTGATCCTGT TCTCTGTCTT CCCGGGAGCA GTAAGCCACC 900
TCTTTCTTTC CCAGGTCCCT GGAGACCACC ATGGAGGCGC GTAACATCTG TGTAGACGCT 960
GCCTACGCGC CTACGCACAG GCATGGTCTA GACAACAGTT TGCAGGGAGC AGCTGCAGCA 1020
CAGACAATCA GTGGGCTCAG CCTGACCCGC CCCTCCCCCA TCTCAGGATT CGACTCAAGC 1080
AAATGGCGTG GGAACTGCTC CAAGACACAG GCCGACAGAA GGATGGCAAC AGACGCGCAG 1140
GGAGATGAAA AAGATGCTTG TGGGGGAAGA GGGAGCAAGG CTGCCTCCCT TCCTGCCACC 1200
CCTTCATGCT ACCCAGAGTT GACTGAAGCA AAGGAAGCGT CATGAAGAGG CAGGCCCAGA 1260
AAACCGGAAG CTGCTGCAGG CTTACTAGTA GGGTGAGCAA AGACACAGCT CCCAGGGACA 1320
GACCCCCCTT TCCCTGCCCC ATCCTCCAAT CATCTGGCTG TGCGTCCCTC CAGAGACACG 1380
CCTGCAAGTG GTCCACAAAC ACTCCTCTAG AGGGCCTGCT CAGAGGGATC CCGGCTTCAC 1440
AGTGAGATCT GTGATGATGC CCCAGCTACT CTGGTCTCAG GAAGACTGGG AGCCCAGGTC 1500
CCCCCAGACA CCTGGTCCTC AGGCTGGGGT GCATGGTCCA CTACTCGGTG CCCCAGGAAC 1560
TCAACAGTCC TTGCTTAGCA GTCTCCGGAG CTTTGAATCT GTTAACTCTT CTACATTCTT 1620
CTTCTTCTTT TTTTTTTTTT TTTGAGACAG AGTCTTGCTC TGTTGCCCAG GCTGGAGTGC 1680
AATGGCGCAA TCTCTGCTCA CTGCAACCTC TGCCTCCCGG GCTCAAGTGA TTCTTCTGCT 1740
TCAGCCTCCC AAGTACCTGA GATTACAGGC ATCTACCACC ACACCCAGCT AATTTTTTTT 1800
TTTTTTTTTT GTATTTTTAG TAGAGACAGG GTTTCACCAT GTTGGCCAGG CTGGTCTTGA 1860
ACTCCTGACC TTAGGTAATC CGCCTGCCTT GGCCTCCCAA AGTGCTGGGA TTACAGACAT 1920
GAGCCACCAC ACCTGGCCAA CTCTTCTACA TTCTATCCTC ACAAGTCAGC ACCAGTCCCC 1980
TTAGAACCTG AACTCAACAG GAAGCTCAGA GAGGCAACAA TGAGGGTGAG GGGAGGAGGC 2040
CAGGAAAGAG CAAGAGAGCC CAGCTGGCAC TCCGCCGTCC GCAGGCTGTA GCTGTGCCTG 2100
ATTCTGAAAG CAGGGGGTTC CATTGCTTTG CCAAGCCTGG GGAGCAACTG TGGGCCTCAG 2160
TGTGAGAGGG CCTCACCTGT GGGACAGCTC CCACTGCGTG GCCTGAGTAG GGGGTACCTG 2220
ATCTTACTCT GTCAATTTGG GGCTAAAGTC ATCTCACCCT AAAGCTACCA GGCAACGTGA 2280
GCCCAGATCT CCCAGCAAGG CAGTGAAAGC CAAGCCATCA GAGCCACATA AGGGTTCCAA 2340
GGCTGAAGAT 2350