EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS073-07294 
Organism
Homo sapiens 
Tissue/cell
GM19238 
Coordinate
chr19:11204910-11207580 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
JUN(var.2)MA0489.1chr19:11205882-11205896AAGAAATGAGTCAT+7.12
JUN(var.2)MA0489.1chr19:11207063-11207077ATGACTCATTTCTT-7.12
JUN(var.2)MA0489.1chr19:11207058-11207072AGGAAATGACTCAT+8.12
JUN(var.2)MA0489.1chr19:11205887-11205901ATGAGTCATTTCCT-8.12
SREBF1MA0595.1chr19:11205756-11205766GTGGGGTGAT-6.02
Number of super-enhancer constituents: 40             
IDCoordinateTissue/cell
SE_01022chr19:11203682-11206319Adrenal_Gland
SE_01022chr19:11206333-11207663Adrenal_Gland
SE_12085chr19:11204949-11207773CD3
SE_14622chr19:11198676-11207877CD4_Memory_Primary_7pool
SE_17142chr19:11204971-11207608CD4p_CD225int_CD127p_Tmem
SE_19715chr19:11204867-11207840CD4p_CD25-_Il17p_PMAstim_Th17
SE_20994chr19:11198676-11207604CD8_Memory_7pool
SE_22774chr19:11204855-11208057CD8_primiary
SE_23239chr19:11203891-11206070Colon_Crypt_1
SE_23239chr19:11206100-11207601Colon_Crypt_1
SE_24095chr19:11204989-11205979Colon_Crypt_2
SE_24095chr19:11206366-11207012Colon_Crypt_2
SE_24095chr19:11207130-11207564Colon_Crypt_2
SE_24928chr19:11205061-11206082Colon_Crypt_3
SE_24928chr19:11206201-11206876Colon_Crypt_3
SE_26902chr19:11204916-11207828Esophagus
SE_28429chr19:11198835-11207741Fetal_Intestine
SE_29308chr19:11199027-11207595Fetal_Intestine_Large
SE_29905chr19:11204956-11208148Fetal_Muscle
SE_31737chr19:11204927-11207763Gastric
SE_34726chr19:11198191-11208606HeLa
SE_36050chr19:11204941-11207563HMEC
SE_38264chr19:11198668-11208150HUVEC
SE_40068chr19:11198411-11207591K562
SE_42817chr19:11199051-11207805Lung
SE_44493chr19:11205013-11206118NHDF-Ad
SE_44493chr19:11206328-11207705NHDF-Ad
SE_44932chr19:11205113-11207883NHLF
SE_47693chr19:11204994-11205972Pancreas
SE_47693chr19:11206368-11206786Pancreas
SE_47693chr19:11207237-11207566Pancreas
SE_49361chr19:11205119-11206191Right_Atrium
SE_49361chr19:11206197-11207709Right_Atrium
SE_50772chr19:11198863-11207767Sigmoid_Colon
SE_52540chr19:11198883-11208401Small_Intestine
SE_54059chr19:11198844-11207806Spleen
SE_57847chr19:11205007-11205595VACO_503
SE_64571chr19:11204940-11207695NHEK
SE_65732chr19:11198652-11207882Pancreatic_islets
SE_68998chr19:11207123-11207544H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr191120695311207150
chr191120569611206011
Enhancer Sequence
TCCTGGTTCA AGCGATTCTC CTGCCTCAGC CTCCTGAGTA GCTGGGATTA CAGGCATGCA 60
CCACCACGCC CGGCTAATTT TGTATTTTTC GTAGAGATGG GGTTTCTCCA CATTGGTTCA 120
GGCTGTTCTC GAACTCCCAA CCTCAGGTGA TCCACCCGCC TCAGCCTCCC AAAGTGCTGG 180
GATTATAGGC GTGAGCCCCC GAACCCGGCC ACTCCCAGCT AAGTTTAAAT TTTTTGTTTG 240
TTTGTTCGTT TGTTTTTATT TTTTGAGACA GAGTCTCCCG CCCAGGCTGG AGCGCAGATC 300
ACTGCATCCT TGACCTCCCA GGCTTAAGCC ATCCTCCCCA CTCAGCCTCC CAAGTAGCTG 360
GGATTACAGG TGTGTGCCAC TATGCTTGGC TAAGTTGTGT ATTTTTTGTA GAGATGGGGT 420
TCAAGGGATT CTCGCTTTGT TGCCTCGGTT GGTCTCAAAC TCCTGGGCTC AAGCAGTCCT 480
CCCTCCTCAG CCTCCCAAGG TGCTGGGGAA ATCCACTTTT GAAACATTGT CTGGAGAGTT 540
GCCCAGGTGG TAGATCACAG AAATAGGTCA TCGTGGGGTC CTTCCCATGG GTGCAGTCTT 600
GAGCCACCTG TGGCCAGCAA ATATTTGGAG AATAATAGTC AGGGGAGAGC TTGAGGTCCA 660
GGGAAAGGTT TTGTTTTTCT TCAGGGAAAG GTTTTTATTG TTCTTTATCC CTCCTTAAAG 720
GACCTTCAGG TGTTACTGAC ATTCCCGGTC TACCCAGTGG CACATTTAGT TTGTAAGCTG 780
GGCCCTCGTA CAGAGGTAGG GAGGTGAGAG CATTGGATTA GTGGTCACCA AAGCTGCGGT 840
CACCTAGTGG GGTGATCAGA GGCTCCTCCC TTAAGATCTT GATTGCCAAC GCCTCTGGCC 900
CAACTTTCCT TTTTATTTAT CGCAAGCCTC CTGGAATCTC AATTGCTTTT TGCCCACCCG 960
GTGTGTCAGC ACAAGAAATG AGTCATTTCC TCCTTTAAGC ACAGTTGAAA TTGAGCTGTG 1020
AGTCAGTGAG GTGTGTACGA TATTGTCAAA GCGGGGTGTG TACAGTATTG ACAGATCTGT 1080
AGTTGGGCAA GAGAATTATC AGAGTTTGTG ACCACAGCAG ATTCCAAAGC TCGACTCATT 1140
TTCTTCTCTC TTCCTTCCCT TTTTTCTTTT CTTTTTTTTT TTTTTTTTGA CAGAGTCTCG 1200
CTCTGTTGCC CAGGCTGGAG TGCAGTGGCA CAATCTGGGC TCACTGCAGC CCCTGCCTCC 1260
TGGGTTCAAA TGATTCTCAT GTTTCAGCCT CCCGAGTAGC TGCAATTACA GGCATTCGGG 1320
TTCAAGTGAT TCTCCTGCCT CAGCCACCTG AGCAGCTGGG ATTACAGGCG CCCGCCACCA 1380
CGCCCGGCTA ATTTTTGTAT TTTTAGTAGA GACGGGGTTT CACCATGTTG GCCAGGCTGG 1440
TCTCGAACTC CTGAACTCAG GTGATCCGCC CACTTCGGCC TCCCAAAGTG CTGAGATTAC 1500
AGACGTGAGT CACCGCGCCC AGCCTGTTCT GTTCTTTAAT TCTCAAAACA CCCTCTAGGA 1560
AGTAGAGACT GCCATTCTCC CCCATTTTAC AGATCAGGAA ACTGAGTCCC AGAAGGATTT 1620
AGTCAGTTAC CCAAGTTGTT CTAGTTAAAT GGCCTGGAAA GCCAGTGAAG CCCAGGATTG 1680
TCTATCTAAC CCCCTTACTA CTCTAACTTT CAGGGAATCC ACATGAATGT GCTGGGTCAA 1740
CCATCAAAGT TGAAATGGAT AAAGGGGGCT GGATGCGGTG GCTGATGCCT GTAATCCTAG 1800
CACTTTGGGA GGCCGAGATG GGTGGGTGGA TTGCTTGAGC CCAAGAGTTT GAGACCAGCC 1860
TGGGCAACAT AGTGAGACAC CTGTCTCTGC AAAAAATAAA TAAAAAGTTA GCTGAGTGTG 1920
ATGGTGCACC CCTCTAGTCA CAGCTGTTGA GTTAGGCTTA GGCAGGAGGA TCGCATGAAC 1980
CTGGGAGGTG GAGGCGGCCG TGAGCCTCAG TCATGCCACT GCACTCCAAC CTGGGCAACA 2040
GAGTGAAAGC CGGTGTCCGA AAGAGAAAGA AAAAAAGACA TAGATACATC TTTTAAAGTT 2100
AGGTTGTATG TTAATTACCT ACAACTCAGT TTCAACTGTG CTTAAAGGAG GAAATGACTC 2160
ATTTCTTGCT ACATATCAAA TTAGCCCAAA ATGTAGTGGC TTAAAACAAC ACATTTATGA 2220
TTTCTCAGTT TTTGCGTGTC AGGAATTTGG AAGCAGCACA GCTAGACGGT TCCAGCTCAG 2280
GGTCTCTCAT GAAGTTGCAA TCAAAATATT GGCAGGAGAG AAAAACATAT TTTCAGAAGC 2340
TGCAGGCATA GGAAGACTTG GCTGGGGTTG AAGGATCCAC TTCCAAGATG GCGCACTCAG 2400
TGGCTCTTGG CTGGAGGCCT CAGTTCCCTG CTGCGTGGAG CTCTCCCTCC AGCTGCTTGA 2460
GTGGACTCAT GACATGCAGC TGGCCTCCCC TGGAGCAGTC GATCCAACAA TGAGCATGGC 2520
CATGAACTAG GCTCAGAAGC CACTCCCTGT CGTCTCTACA TTTTCCTATC AGAAGCAAGT 2580
CATTAAAAGT CCAGTGCCAC TCCAGGGGAG ACGAATTAGG CTCTGCCTTC TGAAAGGATT 2640
ATCACAGAAG ATGCGGTCCT ATATTCTTTT 2670